Investor Presentation - Q3 FY19, February 2019

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Q
3
 
FY19, 
February 
201
9
D
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/
 
I
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THIS PRESENTATION (PRESENTATION) 
IS 
NOT AN OFFER TO 
SELL ANY 
SECURITIES OR 
A 
SOLICITATION TO 
BUY ANY 
SECURITIES OF NATCO PHARMA LIMITED OR
ITS 
SUBSIDIARIES OR JOINT 
VENTURES (TOGETHER, THE
 
“COMPANY”).
The 
material that 
follows 
is a Presentation of general background information about the 
Company’s 
activities as at the date 
of 
the Presentation 
or as otherwise 
indicated. It is
information 
given in 
summary form 
and does 
not 
purport 
to 
be 
complete 
and 
it cannot 
be guaranteed 
that such information 
is 
true 
and 
accurate. 
This 
Presentation 
has been prepared
by and is 
the sole 
responsibility 
of the 
Company. 
By accessing this Presentation, 
you are agreeing 
to 
be bound by 
the 
trading 
restrictions. It 
is 
for 
general 
information purposes 
only
and
 
should
 
not
 
be
 considered
 
as
 
a
 
recommendation
 
that
 
any
 
investor 
should
 
subscribe
 
/ purchase
 
the
 
Company
 
shares.
This 
Presentation includes statements that are, or may be deemed to be, “forward-looking statements”. 
These 
forward-looking statements can 
be 
identified 
by 
the use of forward-
looking 
terminology, 
including the terms 
“believes”, 
“estimates”, “anticipates”, “projects”, 
“expects”, 
“intends”, 
“may”, 
“will”, 
“seeks” or “should” or, in each case, their 
negative 
or other
variations or 
comparable 
terminology, or by 
discussions of 
strategy, 
plans, aims, objectives, goals, future 
events or 
intentions. 
These forward-looking 
statements include 
all 
matters
that 
are 
not historical facts. 
They appear in a 
number of places throughout this Presentation 
and 
include statements 
regarding 
the 
Company’s 
intentions, beliefs or current 
expectations
concerning,
 
amongst
 
other
 
things,
 
its results
 
or 
operations,
 
financial
 
condition,
 
liquidity,
 
prospects,
 
growth, 
strategies
 
and
 
the
 
industry
 
in
 
which
 
the
 
Company
 
operates.
By 
their 
nature, forward-looking statements 
involve 
risks 
and 
uncertainties because they 
relate 
to 
events and depend on 
circumstances 
that may 
or 
may not occur 
in 
the future.
Forward-looking 
statements 
are 
not 
guarantees 
of future performance including those relating to 
general 
business 
plans and 
strategy 
of the 
Company, 
its future outlook 
and growth
prospects, 
and 
future 
developments in 
its 
businesses and 
its competitive 
and regulatory environment. No 
representation, 
warranty 
or undertaking, express or 
implied, 
is 
made 
or
assurance 
given 
that such statements, 
views, 
projections 
or 
forecasts, if 
any, are 
correct 
or 
that the 
objectives 
of the 
Company 
will be achieved. There are 
some important factors that
could cause material differences to 
Company’s 
actual results. 
These 
include 
(i) 
our ability 
to successfully implement 
our 
strategy 
(ii) our growth and expansion plans (iii) 
changes 
in
regulatory 
norms applicable to the Company 
(iv) technological 
changes 
(v) 
investment 
and 
business income 
(vi) 
cash flow projections etc. 
(vii) exposure 
to market 
as well as other
risks.
The Company, as 
such, makes 
no 
representation 
or warranty, express or 
implied, 
as 
to, 
and does 
not accept 
any responsibility or liability with respect 
to, the fairness, 
accuracy,
completeness 
or 
correctness of 
any 
information 
or opinions 
contained 
herein. The 
information contained 
in 
this Presentation, unless 
otherwise 
specified 
is only 
current 
as 
of the 
date 
of
this Presentation. 
The 
Company assumes 
no responsibility 
to publicly amend, modify 
or revise any forward 
looking statements, 
on 
the basis of 
any 
subsequent 
development,
information
 
or
 
events,
 
or
 otherwise.
 
Unless
 
otherwise
 
stated
 
in
 
this
 
Presentation,
 
the
 
information
 
contained
 
herein
 
is
 
based
 
on
 
management
 
information
 
and
 
estimates.
Any 
opinions expressed in 
this presentation 
are 
subject to change 
without 
notice. 
The 
presentation should not 
be 
construed 
as legal, tax, 
investment 
or other advice. None 
of the
Company 
or any 
of its affiliates, 
advisers or representatives 
accepts 
any liability whatsoever 
for 
any 
loss 
howsoever 
arising from 
any 
information presented 
or 
contained 
in 
this
presentation. The 
information contained 
in 
this presentation 
has 
not 
been independently verified. 
Furthermore, 
no 
person 
is 
authorized 
to 
give any 
information 
or 
make 
any
representation which is 
not contained in, 
or 
is inconsistent 
with, 
this presentation. Any such 
extraneous or 
inconsistent 
information 
or 
representation, if 
given or 
made, should not 
be
relied upon as having been authorized by or on behalf 
of the 
Company. 
Further, past performance 
is 
not necessarily 
indicative 
of future
 
results.
This 
document 
is 
just 
a 
Presentation for information purposes 
and private 
circulation 
only and 
is not intended to be a “prospectus” or “offer document” or a 
“private 
placement offer
letter” (as defined or referred to, as the case may be, under the 
Companies 
Act, 2013). It is clarified that this 
Presentation 
is 
not 
intended 
to 
be a 
document offering for subscription 
or
sale of 
any 
securities 
or inviting 
offers from the 
Indian public 
(including 
any 
section thereof) 
or 
from persons residing 
in any other 
jurisdiction including the United States for the
subscription to 
or 
sale of 
any 
securities including the 
equity 
shares of the Company 
or any 
of its subsidiaries. 
No 
part of it should form the basis of 
or be relied upon in 
connection 
with
any investment decision or any 
contract 
or 
commitment to purchase 
or 
subscribe for 
any 
securities. 
None of 
the 
Company’s 
securities 
may be offered or sold in the United States
without
 
registration
 
under
 
the
 
U.S.
 
Securities
 
Act
 
of 
1933,
 
as 
amended,
 
except
 pursuant
 
to
 
an
 
exemption
 
from
 
registration
 
there
 
from.
This 
document 
has 
not 
been and will 
not 
be reviewed or approved by a regulatory 
authority 
in India or by any 
stock 
exchange 
in 
India. 
This presentation is 
confidential 
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this
presentation 
or any 
part thereof should not 
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used 
or relied upon by any other 
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or 
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any other 
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copied, reproduced, 
recirculated, 
redistributed,
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in any 
media, 
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form 
or 
manner, 
in 
part 
or as a whole, without 
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in 
writing 
of the 
Company. 
Any 
unauthorized 
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or
public dissemination 
of information contained 
herein is prohibited. The 
distribution of this presentation 
in 
certain 
jurisdictions 
may 
be 
restricted 
by law. Accordingly, any 
persons 
in
possession
 
of
 
the
 
aforesaid
 
should
 
inform
 
themselves
 
about
 
and
 
observe
 
any
 
such
 
restrictions.
2
N
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P
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a
 
G
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Vertically integrated pharmaceutical company with presence across geographies - India, US  and  ROW
Vertically integrated pharmaceutical company with presence across geographies - India, US  and  ROW
Strong brand position 
Strong brand position 
in the domestic Oncology and Hepatitis – C(‘Hep-C’) segments
in the domestic Oncology and Hepatitis – C(‘Hep-C’) segments
         - Portfolio of brands catering to various oncology diseases including breast, bone, lung and ovarian cancer
         - Portfolio of brands catering to various oncology diseases including breast, bone, lung and ovarian cancer
         - Launched the generic version of Gilead’s Sovaldi (Sofosbuvir) and its combinations for the treatment of Hep-C in India
         - Launched the generic version of Gilead’s Sovaldi (Sofosbuvir) and its combinations for the treatment of Hep-C in India
Focused on 
Focused on 
complex generics for the US Markets
complex generics for the US Markets
 with niche Para IV and Para III filings
 with niche Para IV and Para III filings
Strong focus on R&D 
Strong focus on R&D 
with over 400 employees  dedicated to R&D
with over 400 employees  dedicated to R&D
 
(3)
Total revenues
Total revenues
(1)
 of INR 22,424 mn for the financial year ended 31
 of INR 22,424 mn for the financial year ended 31
st
st
 March 2018
 March 2018
Listed on the BSE and NSE with a market capitalization
Listed on the BSE and NSE with a market capitalization
 
(2)
 of 
USD2.14bn
Incorporated in 1981 and headquartered in Hyderabad with over 4,830 employees across all locations 
Incorporated in 1981 and headquartered in Hyderabad with over 4,830 employees across all locations 
(3)
Expanding into Niche Agrichemical business, leveraging on its Chemistry and manufacturing skills
Expanding into Niche Agrichemical business, leveraging on its Chemistry and manufacturing skills
3
(1)
Represents consolidated 
revenue 
from operations
 
(gross)
(2)
Market 
capitalization as of 
31 March 2018, 
using INR / 
USD exchange 
rate of
 
65.04
(3)
 
As 
of 
March 
31,
 
2018
FY2014
 
and FY2015
 numbers
 
have
 
been prepared
 
under
 
IGAAP,
 
whereas
 
FY2016, FY2017
 
and FY2018
 numbers
 
have
 
been prepared
 
under
 
Ind
 AS
(1)
 
Represents
 
consolidated
 
gross
 
revenue
 
and
 
includes
 
other
 
income
(2)
 
Represents 
PAT after minority
 
interest
(3)
 
Source: 
BSE, 
as of 
December 
3
1
2018
T
r
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R
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d
 
o
f
 
C
o
n
s
i
s
t
e
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t
 
G
r
o
w
t
h
4
1,960
2,131
2,823
6,973
9,688
FY2
0
14
FY2
0
15
FY2
0
16
FY2
0
17
FY2
0
18
1,027
1,346
1,571
6
,9
62
4,860
FY2
0
14
 
FY2
0
15
 
FY2
0
16
 
FY2
0
17
 
FY2
0
18
26%
25%
26%
34%
14%
16%
14%
23%
#
M
argin
s
E
B
I
T
D
A
INRmn
P
A
T
(
2
)
INRm
n
O
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e
(
3
)
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p
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4
 
a
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d
 
h
a
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f
 
y
e
a
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s
(
3
)
Promoters,
48.
42
%
Public, 
           
51.
58
%
43%
31%
K
e
y
 
B
u
s
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s
s
 
S
e
g
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t
s
5
Strategically important
 
division
Vertical 
integration for 
its
Finished 
Dosage 
Formulation
(‘FDF’)
 
portfolio
Filed 
42 DMFs 
in the US 
with
niche 
products under
development
Exports focused on Europe
and 
emerging
 
markets
F
o
r
m
u
l
a
t
i
o
n
s
Operations 
in 
Brazil, Canada,
Singapore and
 
Australia
Selective 
contract 
manufacturing
business 
and other operating
income
O
t
h
e
r
s
A
P
I
(
D
o
m
e
s
t
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c
 
&
 
E
x
p
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s
)
O
v
e
r
v
i
e
w
F
Y
1
8
 
R
e
v
e
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u
e
(
I
N
R
m
n
)
2
,
8
5
4
1
,
9
5
0
F
Y
1
8
 
R
e
v
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u
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C
o
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t
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b
u
t
i
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n
G
r
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t
h
 
F
Y
1
8
o
v
e
r
 
F
Y
1
7
I
n
t
e
r
n
a
t
i
o
n
a
l
Focused on complex 
generics
 
for
the
 US
Front end partnerships with
leading 
global generic 
pharma
companies
Niche 
Para 
IV 
and 
Para III filings
Emerging 
presence 
in Asia,
Europe and developing
 
markets
1
0
,
4
1
8
4
7
%
2
5
%
5
5
%
1
0
%
Note: All 
numbers are 
Gross 
Revenue
All data as of 
March 
31,
 
2018
* 
Includes third party
 
sales
Strong 
brand 
position in the
domestic 
oncology and 
Hepatitis-
C
 
segments
Recent foray 
into the 
Cardiology
and Diabetology
 
segments
Specialist sales 
force of over 350
personnel and over 400
distributors
Fall in FY18 
revenue due 
to
decline 
in 
HepC 
market
 
size.
Expect growth with target
 
launch
of 
8-10 
molecules 
per
 
year
D
o
m
e
s
t
i
c
7
,
2
0
2
*
-
 
1
8
%
3
2
%
1
3
%
9
%
Pipeline of niche and complex generics products in
 
US
29 approved
 
ANDAs
(2)
16 Para IVs 
yet 
to be launched
 
(2)
U
S
 
M
a
r
k
e
t
 
-
 
F
o
c
u
s
 
o
n
 
C
o
m
p
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x
 
G
e
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r
i
c
s
6
K
e
y
 
P
r
o
d
u
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t
s
 
i
n
 
P
i
p
e
l
i
n
e
(1)
Launch 
conditional 
on approval
(2)
As 
of 
March 
31, 2018. 
Approval 
received either by Natco or its 
marketing
 
partner
US 
FDF 
product portfolio is predominantly focused on high-barrier-to-entry products that are typically characterised by one or more of 
the
 
following:
-
Intricate
 
chemistry
-
Challenging delivery
 
mechanism
-
Difficult or complex manufacturing
 
process
-
May face complex legal and regulatory
 
challenges
L
o
w
 
R
i
s
k
 
B
u
s
i
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e
s
s
 
M
o
d
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l
 
t
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r
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u
g
h
 
P
a
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s
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i
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w
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G
l
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P
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a
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i
c
a
l
 
P
l
a
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e
r
s
Adopted and successfully implemented
 
partnership
strategy 
for 
international formulation
 
products
Has product specific partnerships 
with global
 
generic
players 
at different stages of a potential ANDA filing
Low risk business
 
model:
Marketing partner 
typically 
responsible 
for 
the
litigation 
and regulatory process to secure the
ANDA
 
approval
Multi-site
 
approvals
Multi-sourcing
 
arrangements
Profit sharing arrangements 
with 
the front end
partners.
 Brand                             Molecule                         Dosage Form          Therapautic Segment
 
 
S
t
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g
 
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i
n
 
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7
D
o
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F
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(
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)
:
 
M
a
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L
e
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d
i
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g
 
G
r
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t
h
1,983*
2,516*
6,342*
8,810*
7,202*
F
Y
2
0
1
4
F
Y
2
0
1
5
F
Y
2
0
1
6
F
Y
2
0
1
7
F
Y
2
0
1
8
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s
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6
INRm
n
FY2014
 
and
 
FY2015
 
numbers
 
have
 
been
 
prepared
 
under
 
IGAAP,
 
whereas
 
FY2016,
 
FY2017
 
and
 
FY2018
 
numbers
 
have
 
been
 
prepared
 
under
 
Ind
 
AS
(1)
 
Represents gross
 
revenue
*
 
Includes third party
 
sales
D
o
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s
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P
r
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L
a
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F
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U
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Q
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t
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p
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3
5
0
+
 
 Denopsy
 Teriflunomide
Tablets
 Speciality Pharma
Posaconazole
Posan
a
t
 
Injection
 
Speciality Pharma
F
Y
 
1
7
-
1
8
In FY 17-18, Natco had the following product launches
 In the Oncology segment – Alphalan, Carfilnat and Pomalid
 In the Speciality Pharma  segment – Tafnat and Velpanat
 In the Cardiology segment – Arganat and Dabigat
S
t
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a
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P
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s
t
i
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O
n
c
o
l
o
g
y
 
S
e
g
m
e
n
t
8
Entered the segment 
with 
launch of generic version of Imatinib in
 
2003
Portfolio of 
well recognized 
brands – 6 brands 
with 
INR 100mn+ sales in
the oncology
 
segment
P
r
o
g
r
e
s
s
i
v
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w
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d
 
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6
 
i
n
 
2
0
0
3
-
0
4
 
t
o
3
0
(
1
)
Sales 
and marketing of the product 
is 
supported by approximately 70
sales representatives 
and 
strategically located logistics network of
distributors
O
n
c
o
l
o
g
y
 
P
o
r
t
f
o
l
i
o
FY2014
 
and
 
FY2015
 
numbers
 
have
 
been
 
prepared
 
under
 
IGAAP,
 
whereas
 
FY2016,
 
FY2017
 
and
 
FY2018
 
numbers
 
have
 
been
 
prepared
 
under
 
Ind 
AS
(1)
As on 31 March,
 
2018
(2)
Source:
 
Company
O
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c
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y
 
R
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G
r
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B
r
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F
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)
(
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)
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(
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(
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(
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(
B
or
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1,572
1,947
2,526
3,224
3,335
FY2
0
14
 
FY2
0
15
 
FY2
0
16
 
FY2
0
17
 
FY2
0
18
P
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l
t
i
e
s
9
E
x
p
a
n
d
i
n
g
 
I
n
t
o
 
E
m
e
r
g
i
n
g
 
M
a
r
k
e
t
s
 
O
f
 
A
s
i
a
 
A
n
d
 
A
f
r
i
c
a
(1)
 
Including
 
India
G
a
s
t
r
o
 
H
e
p
a
t
o
l
o
g
y
 
L
e
a
d
i
n
g
 
M
a
r
k
e
t
P
o
s
i
t
i
o
n
 
i
n
 
H
e
p
-
C
P
o
r
t
f
o
l
i
o
E
x
t
e
n
d
i
n
g
t
h
e
 
H
e
p
-
C
F
r
a
n
c
h
i
s
e
Launched generic Sofosbuvir and its combinations 
for 
the treatment of Hep-C in India & Nepal under its
 
brand
H
e
p
c
i
n
a
t
 
&
 
H
e
p
c
i
n
a
t
 
L
P
Non-exclusive licensing agreement 
with 
Gilead Sciences 
for 
105 
countries including
 
India
L
a
u
n
c
h
e
d
 
g
e
n
e
r
i
c
 
D
a
c
l
a
t
a
s
v
i
r
 
i
n
 
I
n
d
i
a
 
u
n
d
e
r
 
i
t
s
 
b
r
a
n
d
 
N
a
t
d
a
c
 
a
n
d
 
a
n
 
o
r
a
l
 
f
i
x
e
d
-
d
o
s
e
 
c
o
m
b
i
n
a
t
i
o
n
 
o
f
 
S
o
f
o
s
b
u
v
i
r
a
n
d
 
V
e
l
a
p
a
t
a
s
v
i
r
 
u
n
d
e
r
 
i
t
s
 
b
r
a
n
d
 
V
e
l
p
a
n
a
t
Market 
leading positions 
across the Hep-C class of drugs 
in
 
India
Sales 
and 
marketing 
of the product is supported by approximately 120 sales
 
representatives
L
a
u
n
c
h
e
d
 
H
e
p
c
i
n
a
t
 
P
l
u
s
,
 
a
 
g
e
n
e
r
i
c
 
f
i
x
e
d
 
d
o
s
e
c
o
m
b
i
n
a
t
i
o
n
 
o
f
 
S
o
f
o
s
b
u
v
i
r
 
a
n
d
 
D
a
c
l
a
t
a
s
v
i
r
 
f
o
r
 
t
h
e
f
i
r
s
t
 
t
i
m
e
 
i
n
 
I
n
d
i
a
Foraying 
into RoW
 
markets
Import Permits & Approvals
 
Received
Access 
via 
Agreement 
with
 
Gilead
I
m
p
o
r
t
 
p
e
r
m
i
t
s
 
/
 
a
p
p
r
o
v
a
l
s
 
f
o
r
 
H
e
p
-
C
 
r
e
l
a
t
e
d
 
d
r
u
g
 
r
e
c
e
i
v
e
d
 
i
n
 
1
4
 
c
o
u
n
t
r
i
e
s
(
1
)
E
m
e
r
g
i
n
g
p
o
r
t
f
o
l
i
o
 
o
f
H
e
p
 
B
L
a
u
n
c
h
e
d
 
T
e
n
o
f
o
v
i
r
 
A
l
a
f
e
n
a
m
i
d
e
 
t
a
b
l
e
t
s
u
n
d
e
r
 
i
t
s
 
b
r
a
n
d
 
T
a
f
n
a
t
 
a
s
 
a
n
 
e
x
t
e
n
s
i
o
n
 
t
o
e
x
i
s
t
i
n
g
 
H
e
p
 
B
 
p
o
r
t
f
o
l
i
o
 
o
f
 
T
e
n
o
f
o
v
i
r
(
T
e
r
a
v
i
r
)
 
&
 
E
n
t
e
c
a
v
i
r
 
(
X
-
V
i
r
)
 
t
a
b
l
e
t
s
E
x
p
a
n
d
i
n
g
 
D
o
m
e
s
t
i
c
 
P
r
e
s
e
n
c
e
 
w
i
t
h
 
C
n
D
 
D
i
v
i
s
i
o
n
1
0
C
a
r
d
i
o
l
o
g
y
 
a
n
d
 
D
i
a
b
e
t
o
l
o
g
y
Launched Cardiology and Diabetology (CnD) division in early
 
2017
First to launch Argatroban injection and Dabigatran in India 
for 
treatment of patients 
with 
thrombosis
 
syndrome
Focus 
will 
be on niche molecules 
with 
high barriers to
 
entry
E
x
p
a
n
d
i
n
g
 
R
o
W
 
P
r
e
s
e
n
c
e
1
1
F
o
c
u
s
 
o
n
 
C
a
n
a
d
a
,
 
B
r
a
z
i
l
 
a
n
d
 
o
t
h
e
r
 
R
o
W
 
m
a
r
k
e
t
s
E
u
r
o
p
e
Distribution arrangements 
with 
our
business partner to sell our products
 
in
Eastern Europe, UK and
 
Germany
H
e
p
-
C
 
d
r
i
v
e
n
 
m
a
r
k
e
t
s
Received approvals and import permits 
for
14
 
countries
(1)
(1) Including
 
India
Note: All data as of 
March 
31,
 
2018
Launched Oseltamivir (generic
 
drug
of 
Tamiflu) (30mg, 45mg,
 
75mg)
13
 
approvals
Successful listings in 
major
 
provinces
and retail chains
C
a
n
a
d
a
Commenced 
operations
 
in
2011
Filed multiple
 
oncology
products
Received 
1
st 
product approval
for
 
Letrozole
B
r
a
z
i
l
Presence in Singapore (8 approvals)
 
and
Australia
A
s
i
a
 
P
a
c
i
f
i
c
(
I
n
c
l
u
d
i
n
g
 
A
u
s
t
r
a
l
i
a
)
I
n
-
H
o
u
s
e
 
A
P
I
 
D
e
v
e
l
o
p
m
e
n
t
 
w
i
t
h
 
V
e
r
t
i
c
a
l
 
I
n
t
e
g
r
a
t
i
o
n
 
f
o
r
K
e
y
 
F
o
r
m
u
l
a
t
i
o
n
 
P
r
o
d
u
c
t
s
Strategically important business – 
develops 
APIs primarily 
for 
captive
consumption of its FDF portfolio as 
well 
as third party
 
sales
Portfolio of 42 US 
DMFs
(1) 
with with 
niche products under
 
development
Focuses on complex molecules in oncology and CNS
 
segments
Other therapeutic areas of 
focus 
includes Anti-asthmatic, Anti-
depressant, Anti-migraine, Anti-osteoporosis and G I
 
Disorders
Exports are focused on the US, EU, Canada, Latin America and South-
East
 
Asia
Vertical integration 
for 
several APIs a 
key 
competitive
 
advantage
A
P
I
 
S
t
r
e
n
g
t
h
s
Complex multi-step 
synthesis 
&
 
scale-up
Semi-synthetic fusion technologies
Fermentation / Biotech / 
Synthetic 
/ Separation technologies
Containment / High potency
 
APIs
Peptide 
(Solid 
phase)
 
pharmaceuticals
1
2
E
x
p
a
n
s
i
o
n
 
p
l
a
n
s
 
t
o
 
a
u
g
m
e
n
t
 
A
P
I
 
m
a
n
u
f
a
c
t
u
r
i
n
g
 
c
a
p
a
c
i
t
y
(1) 
As 
of 
March 
31,
 
2018
R
e
s
e
a
r
c
h
 
&
 
D
e
v
e
l
o
p
m
e
n
t
 
C
a
p
a
b
i
l
i
t
i
e
s
1
3
2
9
 
A
N
D
A
s
 
A
p
p
r
o
v
e
d
(
2
)
4
2
 
U
S
 
D
M
F
s
 
F
i
l
e
d
(
2
)
S
e
v
e
r
a
l
 
I
n
t
e
r
n
a
t
i
o
n
a
l
 
a
n
d
I
n
d
i
a
n
 
p
a
t
e
n
t
s
 
f
i
l
e
d
 
a
n
d
g
r
a
n
t
e
d
FY2014 and FY2015 numbers have been prepared under IGAAP, whereas FY2016 and 
FY2017 
numbers
 
have been prepared under 
Ind 
AS
(1) 
As 
of 
March 
31,
 
2018.
(2) 
As 
of 
March 
31, 
2018. Approval 
received either by Natco or its 
marketing
 
partner
#
% 
of standalone
 
revenues
O
v
e
r
 
3
5
 
R
&
D
 
l
a
b
o
r
a
t
o
r
i
e
s
 
i
n
 
2
 
r
e
s
e
a
r
c
h
 
f
a
c
i
l
i
t
i
e
s
Note: 
Rounded 
off to the nearest
 
decimal
Note: Rounded off to the nearest
 
decimal
1
6
 
P
a
r
a
 
I
V
s
 
t
o
 
b
e
 
L
a
u
n
c
h
e
d
(
2
)
39%
39%
4%
5%
3%
10%
Process
De
v
el
o
p
m
e
n
t
Analytical
De
v
el
o
p
m
e
n
t
DQA
Biotech
 
&
Fermentation
Nanoformulations
Discovery
11%
59%
30%
PhD
M
a
s
t
e
rs
Others
C
o
m
m
i
t
m
e
n
t
 
t
o
 
M
a
n
u
f
a
c
t
u
r
i
n
g
 
E
x
c
e
l
l
e
n
c
e
 
w
i
t
h
 
a
 
C
u
l
t
u
r
e
o
f
 
Q
u
a
l
i
t
y
 
a
n
d
 
C
o
m
p
l
i
a
n
c
e
Under
 
development
E
x
p
e
r
i
e
n
c
e
d
 
M
a
n
a
g
e
m
e
n
t
1
5
D
r
.
 
L
i
n
g
a
 
R
a
o
President (Technical
 
Affairs)
M
r
.
 
V
.
C
 
N
a
n
n
a
p
a
n
e
n
i
C
h
a
i
r
m
a
n
 
a
n
d
 
M
a
n
a
g
i
n
g
D
i
r
e
c
t
o
r
Holds 
Masters 
degree in Pharmaceutical Administration from the Long Island 
University,
 
USA
Over 4 
decades of 
experience in 
the pharmaceutical
 
industry
M
r
.
 
R
a
j
e
e
v
 
N
a
n
n
a
p
a
n
e
n
i
Vice 
Chairman 
&
 
CEO
Holds bachelors degree in 
Quantitative 
Economics and History from 
Tufts University, 
Boston,
 
USA
Has 15 years 
of 
experience in 
the 
pharmaceutical
 
industry
Holds 
Masters degree in 
Science 
(Applied 
Chemistry) & Ph.D 
in 
Chemistry from 
JNTU,
 
Hyderabad
Over 4 
decades of 
experience in 
the pharmaceutical industry 
and has been working with 
Natco for 
over 23
 
years
M
r
.
 
P
.
S
.
R
.
K
 
P
r
a
s
a
d
E
x
e
c
u
t
i
v
e
 
V
i
c
e
 
P
r
e
s
i
d
e
n
t
(
C
o
r
p
.
 
E
n
g
i
n
e
e
r
i
n
g
 
S
e
r
v
i
c
e
s
)
Holds 
B.E. 
Mech. 
Engg. from 
Andhra University,
 
Visakhapatnam
Responsible for looking after 
the general administration, engineering, regulatory, training, environmental 
matters, safety, 
health,
production 
and maintenance 
activities of the
 
Company
M
r
.
 
R
a
j
e
s
h
 
C
h
e
b
i
y
a
m
V
i
c
e
 
P
r
e
s
i
d
e
n
t
 
-
 
A
c
q
u
i
s
i
t
i
o
n
s
,
I
n
s
t
i
t
u
t
i
o
n
a
l
 
I
n
v
e
s
t
o
r
 
M
g
m
t
.
 
&
C
o
r
p
o
r
a
t
e
 
C
o
m
m
u
n
i
c
a
t
i
o
n
s
M
r
.
 
S
.
V
.
V
.
N
.
A
p
p
a
 
R
a
o
CFO
Over 27 years 
of 
experience 
including 
22 years within 
the Company 
covering areas 
of accounting, financial controller,
 
treasury
Responsible for finance 
and 
treasury functions at the
 
Company
Holds 
MBA 
from Babson College (USA) 
and Masters degree in 
Chemical 
Engineering 
from 
University 
of 
Rhode
 
Island
20+
 
years 
of
 
experience
 
across
 
supply
 
chain,
 
operations,
 
business
 
development,
 
sales
 
and
 
strategy
D
r
.
 
P
u
l
l
a
 
R
e
d
d
y
 
M
E
x
e
c
u
t
i
v
e
 
V
i
c
e
 
P
r
e
s
i
d
e
n
t
 
-
R
&
D
Holds 
Masters 
in Science (Chemistry) 
and 
Ph.D 
in 
Chemistry, 
both 
from 
University 
of 
Hyderabad. Did 
postdoctoral research
 
for
2.5 
years 
at 
University 
of Zurich,
 
Switzerland
24 years experience 
at Natco 
with 
key 
role in developing novel 
commercially 
viable 
processes for 
over 100 
APIs 
and
intermediates
Holds 
M. 
Pharm and Ph.D. (Pharmaceutics) degree from Nagpur
 
University
32 years 
of 
experience in 
the Pharmaceutical Formulation industry. Responsible for Formulation 
plant 
operations, Product
development and Regulatory
 
compliance
D
r
.
 
R
a
m
i
 
R
e
d
d
y
 
B
Director -
 
Formulations
Bachelors in Commerce and Law from Andhra University, Fellow Member of Institute of Company Secretaries of India
(ICSI)
Over 34 years of experience including 25 years with the Company in legal, secretarial, corporate affairs and patent litigation areas
M
.
 
A
d
i
n
a
r
a
y
a
n
a
Company 
Secretary &
VP-Legal 
& 
Corporate
 
Affairs
N
a
t
c
o
s
 
N
e
a
r
 
a
n
d
 
L
o
n
g
-
T
e
r
m
 
G
o
a
l
s
1
6
D
o
m
e
s
t
i
c
 
B
r
a
n
d
e
d
 
F
o
r
m
u
l
a
t
i
o
n
s
N
e
a
r
-
t
e
r
m
S
t
r
a
t
e
g
i
e
s
L
o
n
g
-
t
e
r
m
S
t
r
a
t
e
g
i
e
s
D
e
m
o
n
s
t
r
a
t
e
d
 
T
r
a
c
k
 
R
e
c
o
r
d
 
o
f
 
T
o
p
l
i
n
e
 
a
n
d
 
E
a
r
n
i
n
g
s
G
r
o
w
t
h
P
A
T
(
2
)
 
(
I
N
R
m
n
)
 
a
n
d
 
P
A
T
 
M
a
r
g
i
n
 
(
%
)
1
7
R
O
E
 
(
%
)
R
O
C
E
 
(
%
)
1,027
1,346
1,571
FY2
0
14
FY2
0
15
FY2
0
16
FY2
0
17
FY2
0
18
1
3
.
6
%
1
6
.
0
%
14.2%
 
15.9%
12.0%
29.5%
22.6%
FY2
0
14
FY2
0
15
FY2
0
16
FY2
0
17
FY2
0
18
18.7%
17.1%
16.9%
38.0%
28.9%
FY2
0
14
FY2
0
15
FY2
0
16
FY2
0
17
FY2
0
18
(1)
Represents consolidated gross 
revenue and 
includes other
 
income
(2)
Represents 
PAT 
after minority
 
interest
F
Y
2
0
1
4
 
a
n
d
 
F
Y
2
0
1
5
 
n
u
m
b
e
r
s
 
h
a
v
e
 
b
e
e
n
 
p
r
e
p
a
r
e
d
 
u
n
d
e
r
 
I
G
A
A
P
,
 
w
h
e
r
e
a
s
 
F
Y
2
0
1
6
 
a
n
d
 
F
Y
2
0
1
7
 
n
u
m
b
e
r
s
 
h
a
v
e
 
b
e
e
n
 
p
r
e
p
a
r
e
d
 
u
n
d
e
r
 
I
n
d
 
A
S
1
4
.
4
%
2
3
.
4
%
3
1
.
0
%
6
,9
62
4,860
H
i
s
t
o
r
i
c
a
l
 
F
i
n
a
n
c
i
a
l
s
C
o
n
s
o
l
i
d
a
t
e
d
 
P
r
o
f
i
t
 
&
 
L
o
s
s
 
S
t
a
t
e
m
e
n
t
 
(
I
N
R
m
n
)
1
8
FY2014 and FY2015 numbers have been prepared under IGAAP, whereas FY2016 and 
FY2017 
numbers
 
have been prepared under 
Ind 
AS
S
e
g
m
e
n
t
a
l
 
B
r
e
a
k
d
o
w
n
 
(
I
N
R
 
M
n
)
H
i
s
t
o
r
i
c
a
l
 
F
i
n
a
n
c
i
a
l
s
 
(
c
o
n
t
d
.
)
C
o
n
s
o
l
i
d
a
t
e
d
 
F
i
n
a
n
c
i
a
l
 
R
e
s
u
l
t
s
 
(
I
N
R
 
M
n
)
Note: The 
Company adopted 
Indian Accounting 
Standards 
("Ind 
AS") 
from 
1 
April 
2016 and 
prior period figures 
have been 
reclassified 
wherever 
required to conform to the classification of the current
 
period.
1
9
 
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This presentation by Natco Pharma Limited provides general background information about the company's activities as of the presentation date. It includes forward-looking statements that involve risks and uncertainties, discussing the company's intentions, beliefs, and expectations. The material serves for general information purposes only and does not constitute an offer to sell securities or investment advice.

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  1. INVESTOR PRESENTATION Q3 FY19, February 2019

  2. Disclaimer / Important Disclosure THIS PRESENTATION (PRESENTATION) IS NOT AN OFFER TO SELL ANY SECURITIES OR A SOLICITATION TO BUY ANY SECURITIES OF NATCO PHARMA LIMITED OR ITS SUBSIDIARIES OR JOINT VENTURES (TOGETHER, THE COMPANY ). The material that follows is a Presentation of general background information about the Company s activities as at the date of the Presentation or as otherwise indicated. It is information given in summary form and does not purport to be complete and it cannot be guaranteed that such information is true and accurate. This Presentation has been prepared by and is the sole responsibility of the Company. By accessing this Presentation, you are agreeing to be bound by the trading restrictions. It is for general information purposes only and should not be consideredas a recommendationthat any investor should subscribe/ purchase the Company shares. This Presentation includes statements that are, or may be deemed to be, forward-looking statements . These forward-looking statements can be identified by the use of forward- looking terminology, including the terms believes , estimates , anticipates , projects , expects , intends , may , will , seeks or should or, in each case, their negative or other variations or comparable terminology, or by discussions of strategy, plans, aims, objectives, goals, future events or intentions. These forward-looking statements include all matters that are not historical facts. They appear in a number of places throughout this Presentation and include statements regarding the Company s intentions, beliefs or current expectations concerning, amongst other things, its results or operations, financial condition,liquidity, prospects, growth, strategies and the industry in which the Company operates. By their nature, forward-looking statements involve risks and uncertainties because they relate to events and depend on circumstances that may or may not occur in the future. Forward-looking statements are not guarantees of future performance including those relating to general business plans and strategy of the Company, its future outlook and growth prospects, and future developments in its businesses and its competitive and regulatory environment. No representation, warranty or undertaking, express or implied, is made or assurance given that such statements, views, projections or forecasts, if any, are correct or that the objectives of the Company will be achieved. There are some important factors that could cause material differences to Company s actual results. These include (i) our ability to successfully implement our strategy (ii) our growth and expansion plans (iii) changes in regulatory norms applicable to the Company (iv) technological changes (v) investment and business income (vi) cash flow projections etc. (vii) exposure to market as well as other risks. The Company, as such, makes no representation or warranty, express or implied, as to, and does not accept any responsibility or liability with respect to, the fairness, accuracy, completeness or correctness of any information or opinions contained herein. The information contained in this Presentation, unless otherwise specified is only current as of the date of this Presentation. The Company assumes no responsibility to publicly amend, modify or revise any forward looking statements, on the basis of any subsequent development, information or events, or otherwise. Unless otherwise stated in this Presentation, the information contained herein is based on management information and estimates. Any opinions expressed in this presentation are subject to change without notice. The presentation should not be construed as legal, tax, investment or other advice. None of the Company or any of its affiliates, advisers or representatives accepts any liability whatsoever for any loss howsoever arising from any information presented or contained in this presentation. The information contained in this presentation has not been independently verified. Furthermore, no person is authorized to give any information or make any representation which is not contained in, or is inconsistent with, this presentation. Any such extraneous or inconsistent information or representation, if given or made, should not be relied upon as having been authorized by or on behalf of the Company. Further, past performance is not necessarily indicative of futureresults. This document is just a Presentation for information purposes and private circulation only and is not intended to be a prospectus or offer document or a private placement offer letter (as defined or referred to, as the case may be, under the Companies Act, 2013). It is clarified that this Presentation is not intended to be a document offering for subscription or sale of any securities or inviting offers from the Indian public (including any section thereof) or from persons residing in any other jurisdiction including the United States for the subscription to or sale of any securities including the equity shares of the Company or any of its subsidiaries. No part of it should form the basis of or be relied upon in connection with any investment decision or any contract or commitment to purchase or subscribe for any securities. None of the Company s securities may be offered or sold in the United States without registrationunder the U.S. Securities Act of 1933, as amended, except pursuant to an exemption from registration there from. This document has not been and will not be reviewed or approved by a regulatory authority in India or by any stock exchange in India. This presentation is confidential and this presentation or any part thereof should not be used or relied upon by any other party or for any other purpose and should not be copied, reproduced, recirculated, redistributed, published in any media, website or otherwise, in any form or manner, in part or as a whole, without the express consent in writing of the Company. Any unauthorized use, disclosure or public dissemination of information contained herein is prohibited. The distribution of this presentation in certain jurisdictions may be restricted by law. Accordingly, any persons in possession of the aforesaid should inform themselves about and observe any such restrictions. 2

  3. Natco Pharma at a Glance Represents consolidated revenue from operations (gross) Market capitalization as of 31 March 2018, using INR / USD exchange rate of 65.04 As of March 31, 2018 Represents consolidated revenue from operations (gross) Vertically integrated pharmaceutical company with presence across geographies - India, US and ROW Market capitalization as of 31 March 2018, using INR / USD exchange rate of 65.04 Strong brand position in the domestic Oncology and Hepatitis C( Hep-C ) segments - Portfolio of brands catering to various oncology diseases including breast, bone, lung and ovarian cancer - Launched the generic version of Gilead s Sovaldi (Sofosbuvir) and its combinations for the treatment of Hep-C in India As of March 31, 2018 Focused on complex generics for the US Markets with niche Para IV and Para III filings Strong focus on R&D with over 400 employees dedicated to R&D(3) Expanding into Niche Agrichemical business, leveraging on its Chemistry and manufacturing skills Total revenues(1) of INR 22,424 mn for the financial year ended 31st March 2018 Listed on the BSE and NSE with a market capitalization (2) of USD2.14bn Incorporated in 1981 and headquartered in Hyderabad with over 4,830 employees across all locations (3) 3 (1) (2) Represents consolidated revenue from operations(gross) Market capitalization as of 31 March 2018, using INR / USD exchange rate of 65.04

  4. Track Record of Consistent Growth Strong Revenue(1)Growth OwnershipStructure(3) INRmn 22,424 20,789 10,897 8,402 7,556 Promoters, 48.42% Public, 51.58% FY2014 FY2015 FY2016 FY2017 FY2018 And Robust EBITDA and PAT(2)Margins EBITDA INRmn 26% 25% 26% 34% 43% Natco Pharma s Stock Performance over the past 4 and half years(3) 9,688 6,973 2,823 2,131 1,960 FY2014 FY2015 FY2016 FY2017 FY2018 PAT(2) INRmn 16% 14% 31% 14% 23% 6,962 4,860 1,571 1,346 1,027 FY2014 FY2015 FY2016 FY2017 FY2018 4 FY2014and FY2015numbershavebeen preparedunderIGAAP, whereasFY2016, FY2017and FY2018numbershavebeen preparedunderInd AS (1) Representsconsolidatedgrossrevenueand includesotherincome (2) Represents PAT after minorityinterest (3) 2018 Source: BSE, as of December 31 # Margins

  5. Key Business Segments Formulations API Others (Domestic &Exports) Domestic International Operations in Brazil, Canada, Singapore and Australia Strong brand position in the domestic oncology and Hepatitis- C segments Recent foray into the Cardiology and Diabetology segments Specialist sales force of over 350 personnel and over 400 distributors Fall in FY18 revenue due to decline in HepC market size. Expect growth with target launch of 8-10 molecules per year Focused on complex generics for the US Front end partnerships with leading global generic pharma companies Niche Para IV and Para III filings Emerging presence in Asia, Europe and developing markets Strategically important division Vertical integration for its Finished Dosage Formulation ( FDF )portfolio Filed 42 DMFs in the US with niche products under development Exports focused on Europe and emerging markets Selective contract manufacturing business and other operating income Overview FY18Revenue (INRmn) 7,202* 10,418 2,854 1,950 13% FY18Revenue Contribution 9% 32% 47% - 18% GrowthFY18 over FY17 25% 55% 10% 5 Note: All numbers are Gross Revenue All data as of March 31, 2018 * Includes third partysales

  6. US Market - Focus on Complex Generics US FDF product portfolio is predominantly focused on high-barrier-to-entry products that are typically characterised by one or more of thefollowing: - Intricate chemistry - Challenging delivery mechanism - Difficult or complex manufacturingprocess - May face complex legal and regulatorychallenges Key Products in Pipeline Low Risk Business Model through Partnerships with Global PharmaceuticalPlayers Key Brand Molecule Therapeutic Segment / Indication Para IV Adopted and successfully implementedpartnership Gilenya Fingolimod Multiple Sclerosis strategy for international formulationproducts Treanda Bendamustine Cancer, CLL Has product specific partnerships with global generic Nexavar Sorafenib Liver, Kidney Cancer players at different stages of a potential ANDA filing Tracleer Bosentan Hypertension Para III To Be Launched Low risk business model: Revlimid(1) Lenalidomide Multiple Myeloma Marketing partner typically responsible for the litigation and regulatory process to secure the ANDA approval Afinitor Everolimus (higher strength) Kidney Cancer Zytiga Abiraterone Prostate Cancer Multi-site approvals Multi-sourcing arrangements Tarceva Erlotinib NSCLC, Pancreatic Cancer Profit sharing arrangements with the front end Kyprolis Carfilzomib Multiple Myeloma partners. Aubagio Teriflunomide Multiple Sclerosis Eliquis Apixaban Anticoagulant Pipeline of niche and complex generics products in US Pomalyst Pomalidomide Multiple Myeloma 29 approved ANDAs(2) Sovaldi Sofosbuvir Anti-Viral / Hep C 16 Para IVs yet to be launched(2) Ibruvika Ibrutinib Cancer 6 (1) Launch conditional on approval (2) As of March 31, 2018. Approval received either by Natco or its marketing partner

  7. Brand Molecule Dosage Form Therapautic Segment Strong Growth in Domestic Formulations Business Domestic Formulation Sales(1): Market LeadingGrowth Domestic Product Launches In FY 17-18, Natco had the following product launches In the Oncology segment Alphalan, Carfilnat and Pomalid In the Speciality Pharma segment Tafnat and Velpanat In the Cardiology segment Arganat and Dabigat INRmn FY 17-18 8,810* Brand Molecule Dosage Form Therapautic Segment 7,202* Denopsy Teriflunomide Posaconazole Tablets Speciality Pharma UPTO Q3 Posanat Injection Speciality Pharma FY19 6,342* Herduo Lapatinib Tablets Oncology Hepcinat Plus Sofosbuvir+ Daclatasvir Tablets SpecialityPharma Strong position in Oncology and Hepatitis-Cdomains Brands in excess of INR100mn+ sales in Oncologysegment 2,516* 6 1,983* Brands occupy the #1 positionin Hep-C segment 4 Sales force in India across Oncology, GastroHepatology, Cardiology and Diabetology FY2014 FY2015 FY2016 FY2017 FY2018 350+ 7 FY2014 and FY2015 numbers have been prepared under IGAAP, whereas FY2016, FY2017 and FY2018 numbers have been prepared under Ind AS (1) Represents gross revenue * Includes third party sales

  8. Strong Market Position in Domestic Oncology Segment Oncology DivisionOverview Oncology Revenue Gross (INRmn) Entered the segment with launch of generic version of Imatinib in 2003 Portfolio of well recognized brands 6 brands with INR 100mn+ sales in 3,335 3,224 the oncology segment 2,526 Progressively widened its oncology product range from 6 in 2003-04 to 1,947 30(1) 1,572 Sales and marketing of the product is supported by approximately 70 sales representatives and strategically located logistics network of distributors FY2014 FY2015 FY2016 FY2017 FY2018 INR100mn+ Brands (FY18)(2) Oncology Portfolio (Veenat) (Lenalid) (Bortenat) Hematology Solid Tumors (Erlonat) (Geftinat) (Sorafenat) # ofActive Brands(1) 13 17 8 FY2014 and FY2015 numbers have been prepared under IGAAP, whereas FY2016, FY2017 and FY2018 numbers have been prepared under Ind AS (1) As on 31 March,2018 (2) Source:Company

  9. Pharma Specialties Launched generic Sofosbuvir and its combinations for the treatment of Hep-C in India & Nepal under its brand Hepcinat & Hepcinat LP Gastro Hepatology Leading Market Position in Hep-C Portfolio Non-exclusive licensing agreement with Gilead Sciences for 105 countries including India Launched generic Daclatasvir in India under its brand Natdac and an oral fixed-dose combination of Sofosbuvir and Velapatasvir under its brand Velpanat Market leading positions across the Hep-C class of drugs in India Sales and marketing of the product is supported by approximately 120 salesrepresentatives Launched Hepcinat Plus, a generic fixed dose combination of Sofosbuvir and Daclatasvir for the first time in India Launched Tenofovir Alafenamide tablets under its brand Tafnat as an extensionto existing Hep B portfolio of Tenofovir (Teravir) & Entecavir (X-Vir) tablets Emerging portfolioof Hep B Extending the Hep-C Franchise Foraying into RoW markets Expanding Into Emerging Markets Of Asia And Africa Import Permits & ApprovalsReceived Access via Agreement withGilead Import permits / approvals for Hep-C related drug received in 14 countries(1) 9 (1) IncludingIndia

  10. Expanding Domestic Presence with CnD Division Cardiology and Diabetology Launched Cardiology and Diabetology (CnD) division in early 2017 First to launch Argatroban injection and Dabigatran in India for treatment of patients with thrombosis syndrome Focus will be on niche molecules with high barriers to entry 10

  11. Expanding RoW Presence Focus on Canada, Brazil and other RoW markets Hep-C driven markets Canada Received approvals and import permits for 14 countries(1) Launched Oseltamivir (genericdrug of Tamiflu) (30mg, 45mg,75mg) 13 approvals Successful listings in major provinces and retail chains Asia Pacific (IncludingAustralia) Presence in Singapore (8 approvals)and Australia Europe Brazil Distribution arrangements with our business partner to sell our productsin Eastern Europe, UK and Germany Commenced operationsin 2011 Filed multipleoncology products Received 1st product approval for Letrozole 11 (1) Including India Note: All data as of March 31,2018

  12. In-House API Development with Vertical Integration for Key Formulation Products Mekaguda Facility Chennai Facility Strategically important business develops APIs primarily for captive consumption of its FDF portfolio as well as third party sales Portfolio of 42 US DMFs(1) with with niche products underdevelopment Focuses on complex molecules in oncology and CNS segments Other therapeutic areas of focus includes Anti-asthmatic, Anti- depressant, Anti-migraine, Anti-osteoporosis and G I Disorders Cytotoxic API s and Biotechnologybased products Complex chemistry peptides Chemistry Skills Exports are focused on the US, EU, Canada, Latin America and South- East Asia Synthetic chemistry Vertical integration for several APIs a key competitiveadvantage GMP, USFDA, German Health Authority, PMDA (Japan), Cofepris (Mexico) Key Regulatory Approvals API Strengths GMP, USFDA Complex multi-step synthesis & scale-up Semi-synthetic fusion technologies Fermentation / Biotech / Synthetic / Separation technologies US FDA audit with Zero observations completed in February 2018 US FDA audit EIR Received August 2016 Last US FDA Audit Containment / High potency APIs Peptide (Solid phase) pharmaceuticals Expansion plans to augment API manufacturingcapacity 12 (1) As of March 31,2018

  13. Research & Development Capabilities R&D capabilitiesdemonstrated by its complex and niche product filings in formulations and API segments 29 ANDAs Approved(2) Two research facilities with capabilities across synthetic chemistry, biotech & fermentation, nano pharmaceuticals, new drug discovery & cell biology R&D Expense (INRmn) and as % of StandaloneRevenue 16 Para IVs to beLaunched(2) 6.7% 6.0% 7.8% 7.1% 6.4% 1,665 1,216 703 517 407 42 US DMFsFiled(2) FY2014 FY2015 FY2016 FY2017 FY2018 Talented Pool of Scientists (Total no:271)(1) Process Development Analytical Development 10% 4% 11% 5% 3% 30% 39% PhD DQA Masters Biotech & Fermentation Others 59% Nanoformulations 39% Several International and Indian patents filed and granted Discovery Note: Rounded off to the nearestdecimal Note: Rounded off to the nearestdecimal Over 35 R&D laboratories in 2 researchfacilities 13 FY2014 and FY2015 numbers have been prepared under IGAAP, whereas FY2016 and FY2017 numbers have been prepared under Ind AS (1) As of March 31,2018. (2) As of March 31, 2018. Approval received either by Natco or its marketingpartner # % of standalone revenues

  14. Commitment to Manufacturing Excellence with a Culture of Quality and Compliance International MarketsFormulations Kothur Facility Visakhapatnam Facility Tablets, Capsules, Pellets, Injectables Cytotoxic & other Oral Solid Dosages Capability Key Regulatory Approvals GMP, USFDA, German Health Authority, ANVISA na Targeted towards US & other International regulated markets Other Highlights Located in a Special Economic Zone (SEZ) US FDA audit EIR Received July 2017 Facility license received. Qualification batches in progress Domestic MarketFormulations Nagarjuna Sagar Facility Dehradun Unit 6 Facility Dehradun Unit 7 Facility Guwahati Facility Ampoules, Vials, Lyophilized vials, Parenterals, Sterile Dry Powders Tablets, Capsules, Injectables Tablets, Capsules Tablets, Capsules Capability Key Regulatory Approvals GMP, Public Health Service of the Netherlands (EU GMP) GMP GMP GMP Compliant Facility 14 Under development

  15. Experienced Management Mr. V.C Nannapaneni Chairman andManaging Director Holds Masters degree in Pharmaceutical Administration from the Long Island University,USA Over 4 decades of experience in the pharmaceuticalindustry Holds bachelors degree in Quantitative Economics and History from Tufts University, Boston,USA Mr. RajeevNannapaneni Vice Chairman & CEO Has 15 years of experience in the pharmaceuticalindustry Mr. P.S.R.K Prasad Executive Vice President (Corp. EngineeringServices) Holds B.E. Mech. Engg. from Andhra University,Visakhapatnam Responsible for looking after the general administration, engineering, regulatory, training, environmental matters, safety, health, production and maintenance activities of theCompany Holds Masters degree in Science (Applied Chemistry) & Ph.D in Chemistry from JNTU,Hyderabad Dr. Linga Rao President (TechnicalAffairs) Over 4 decades of experience in the pharmaceutical industry and has been working with Natco for over 23years Bachelors in Commerce and Law from Andhra University, Fellow Member of Institute of Company Secretaries of India (ICSI) M. Adinarayana Company Secretary & VP-Legal & CorporateAffairs Over 34 years of experience including 25 years with the Company in legal, secretarial, corporate affairs and patent litigation areas Over 27 years of experience including 22 years within the Company covering areas of accounting, financial controller,treasury Mr. S.V.V.N.AppaRao CFO Responsible for finance and treasury functions at theCompany Holds Masters in Science (Chemistry) and Ph.D in Chemistry, both from University of Hyderabad. Did postdoctoral researchfor 2.5 years at University of Zurich, Switzerland Dr. Pulla Reddy M Executive Vice President- R&D 24 years experience at Natco with key role in developing novel commercially viable processes for over 100 APIs and intermediates Holds M. Pharm and Ph.D. (Pharmaceutics) degree from NagpurUniversity Dr. Rami Reddy B Director - Formulations 32 years of experience in the Pharmaceutical Formulation industry. Responsible for Formulation plant operations, Product development and Regulatorycompliance Mr. Rajesh Chebiyam Vice President -Acquisitions, Institutional Investor Mgmt. & Corporate Communications Holds MBA from Babson College (USA) and Masters degree in Chemical Engineering from University of RhodeIsland 20+ years of experience across supply chain, operations,business development, sales and strategy 15

  16. Natcos Near and Long-Term Goals Domestic Branded Formulations Complex Generics & ExportMarkets Focus on growth in key subsidiaries of Canada & Maintain leadership position in Oncology and Brazil Hepatitis-C segment Near-term Strategies Intensify the focus of CnD pipeline forniche Intensify regulatory filings rate in RoWmarkets launches led by Hep-C portfolio Launch 8-10 new products Entered niche agrichemical business Focus on a select few high-potential filings, Enter new attractivesegments predominantly differentiated products througheither Growth through inorganicstrategies Long-term Strategies Novel Drug Delivery Systems (NDDS) or complex chemistries Strategic alliances in RoW markets for furthergrowth 16

  17. Demonstrated Track Record of Topline and Earnings Growth FY2014 and FY2015 numbers have been prepared under IGAAP, whereas FY2016 and FY2017 numbers have been prepared under Ind AS Total Gross Revenue(1)(INRmn) EBITDA (INRmn) and EBITDA Margin (%) 33.5% 25.9% 25.4% 25.9% 43.2% 20,789 22,424 10,897 9,688 8,402 7,556 6,973 2,823 2,131 1,960 FY2014 FY2015 FY2016 FY2017 FY2018 FY2014 FY2015 FY2016 FY2017 FY2018 PAT(2) (INRmn) and PAT Margin (%) ROE (%) ROCE (%) 31.0% 16.0% 14.4% 23.4% 13.6% 38.0% 6,962 29.5% 28.9% 4,860 22.6% 18.7% 15.9% 17.1% 16.9% 14.2% 1,571 1,346 12.0% 1,027 FY2014 FY2015 FY2016 FY2017 FY2018 FY2014 FY2015 FY2016 FY2017 FY2018 FY2014 FY2015 FY2016 FY2017 FY2018 (1) (2) Represents consolidated gross revenue and includes other income Represents PAT after minority interest 17

  18. Historical Financials Consolidated Balance Sheet (INRmn) Particulars ASSETS Non-current assets (a) Property, plant and equipment (b) Capital work-in-progress (c) Intangibleassets (d) Financial assets Investments Other financialassets (e) Current-tax assets (net) (f) Other non-currentassets Consolidated Profit & Loss Statement(INRmn) Particulars Revenue Revenue from operations (Refer note 5) Other income Totalrevenues Expenses Cost of materials consumed Excise duty (Refer note 5) Purchases of stock-in-trade Changes in inventories of finished goods, stock-in -trade and work-in- progress Employee benefits expense Finance costs Depreciation and amortisation expense Other expenses Totalexpenses 31-March-2018 31-March-2017 31-March-2018 31-March-2017 22,020 404 22,424 20,650 139 20,789 10,127 4,800 8,272 3,363 59 58 5,208 448 971 (188) 3,905 172 459 (253) 81 150 18 609 1 131 - 478 15,844 12,303 2,432 185 544 4,945 14,545 3,256 154 662 5,197 13,552 Current assets (a) Inventories (b) Financial Assets Investments Trade receivables Cash and cash equivalents Bank balances other than cash and cash equivalents Loans Other financialassets (c) Other currentassets 4,384 3,489 684 321 6,375 217 1,620 4,752 235 123 Profit beforetax 8,872 6,244 45 35 752 Tax expense / (credit) Current tax Deferred tax Minimum alternative tax credit Tax for earlieryears 6,142 1,840 21,307 37,151 1,354 2,199 1,166 10,873 23,176 1 - - (279) Totalassets 40 - EQUITY AND LIABILITIES Equity (a) Equity share capital (b) Other equity Equity attributable toowners 6,952 4,849 Profit aftertax 369 349 30,353 30,722 16,144 16,493 Other comprehensive income (net of taxes) Items that will not be reclassified to profit orloss Re-measurement gains/(losses) on defined benefit plans Net (loss)/gain on FVTOCI equitysecurities Items that will be reclassified to profit orloss Exchange differences on translation of foreignoperations (42) (2) (50) 28 Non-controlling interest Total ofEquity 38 41 30,760 16,534 (8) (12) Liabilities Non-current liabilities (a) Financial liabilities Other financialliabilities (b) Provision for employee benefits (c) Deferred tax liabilities(net) Total comprehensiveincome 6,900 4,815 8 8 Profit attributableto: Owners of the parent Non-controlling interests 324 139 471 219 150 377 4,860 (11) 6,962 (10) Current liabilities (a) Financial liabilities Borrowings Trade payables Other financialliabilities (b) Other currentliabilities (c) Provision for employeebenefits (d) Current-tax liabilities(net) Total comprehensive income attributableto: Owners of the parent Non-controlling interests 6,910 (10) 4,826 (11) 1,732 2,691 1,024 310 137 2,216 2,627 1,014 257 Paid-up equity share capital of 2each Other equity (Revaluation reserve Nil) 349 369 16,144 30,353 18 133 26 Earnings per share (non-annualised) Basic (in ) Diluted (in ) 5,920 6,265 39.26 39.13 27.78 27.75 Total equity andliabilities 37,151 23,176 18 FY2014 and FY2015 numbers have been prepared under IGAAP, whereas FY2016 and FY2017 numbers have been prepared under Ind AS

  19. Historical Financials (contd.) Consolidated Financial Results (INRMn) Segmental Breakdown (INRMn) Revenue Division Q3FY19 FY18 Q3FY18 FY17 Q3FY19 FY18 Q3 FY18 FY17 Total API Total Revenues 5,800 22,424 5736 20,789 API Gross Revenue 992.5 2,853.9 816.6 1,837.7 Formulation export and profit share 2,573.1 10,419.0 2,890.3 8276.0 EBITDA EBITDA Margin (%) 2317 9,688 2979 6,973 39.9% 43.20% 51.9% 33.50% Formulations Onco (including CnD) 942.5 3,380.6 848.3 3,224.3 Formulations, Brand Pharma Non - Onco Formulations, 3rd party, & miscel PAT (after minority interest) PAT Margin (%) 503.2 3,103.5 685.6 4,801.6 1593 6,962 2174 4,860 195.6 718.2 125.7 784.6 27.5% 31.00% 37.9% 23.40% Formulations Gross Revenue 4,214.4 17,620.9 4,549.9 17,086.1 Other Operating and Non - operating incomes 349.1 1,003.9 148.5 1,236.0 Stand-Alone Total Net Revenue Total Revenue, all subsidiaries 5,556.0 21,479 5,515.0 20,159.8 244.0 945.3 221.0 630.0 Consolidated Total Net Revenue 5,800.0 22,424.0 5,736.0 20789.8 19 Note: The Company adopted Indian Accounting Standards ("Ind AS") from 1 April 2016 and prior period figures have been reclassified wherever required to conform to the classification of the current period.

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