Approval Accorded under PLI Scheme for Promotion of Domestic
Manufacturing of Critical Key Starting Materials (KSMs)/ Drug Intermediates and
APIs
[Min of Chemicals
and Fertilizers Press Release/22.01.2021]
The Applications of following companies, which
have committed more than the minimum proposed annual production capacities and
fulfil the prescribed criteria have been approved under Production Linked Incentive (PLI) Scheme for Promotion of Domestic Manufacturing of critical Key Starting
Materials (KSMs)/Drug Intermediates and Active Pharmaceutical Ingredients
(APIs) in the country:
|
S.No. |
Name of approved Applicant |
Name of Eligible Product |
Committed Production Capacity (in MT) |
Committed Investment (in Rs.
crores) |
|
1. |
M/s Aurobindo
Pharma Limited (through LyfiusPharma Pvt. Ltd.) |
Penicillin G |
15000 |
1392 |
|
2. |
M/s Karnataka Antibiotics &
Pharmaceuticals Ltd. |
7 - ACA |
1000 |
275 |
|
3. |
M/s Aurobindo
Pharma Limited (through LyfiusPharma Pvt. Ltd.) |
2000 |
813 |
|
|
4. |
M/s Aurobindo
Pharma Limited (through Qule Pharma Pvt. Ltd.) |
Erythromycin Thiocyanate (TIOC) |
1600 |
834 |
|
5. |
M/s Kinvan Pvt.
Ltd. |
Clavulanic Acid |
300 |
447.17 |
The setting up of these plants will lead to
total committed investment of Rs. 3,761 cr. by the
companies and employment generation of about 3,825. The commercial production
is projected to commence from 1st April,
2023 and the disbursal of production linked incentive by the Government over
the six years period would be up to a maximum of Rs.
3,600 cr. Setting of these plants will make the country self-reliant to a large
extent in respect of these Bulk drugs.
With an objective to attain self-reliance and
reduce import dependence in these critical Bulk Drugs - Key Starting Materials
(KSMs)/ Drug Intermediates and Active Pharmaceutical Ingredients (APIs) in the
country, the Department of Pharmaceuticals had launched a Production Linked Incentive (PLI) Scheme for promotion of their domestic manufacturing by setting up greenfield
plants with minimum domestic value addition in four different Target Segments
(In Two Fermentation based - at
least 90% and in the Two Chemical
Synthesis based – at least 70% ) with a total outlay of Rs.
6,940 cr. for the period 2020-21 to 2029-30.
The applications under four different Target
Segments were invited with 30th November, 2020 as the last date. In
total, 215 applications have been received for the 36 products spread across
the 4 Target Segments. The guidelines prescribed that the applications would be
processed and decided within a period of 90 days, i.e., up to 28th
February, 2021.
The Target Segment-I includes 4 Eligible
Products, viz., Penicillin G; 7-ACA; Erythromycin Thiocyanate (TIOC) &
Clavulanic Acid, in which the country is presently fully import dependent, were
considered on priority as per the decided evaluation and selection criteria.
Further, applications under the other three
segments are proposed to be taken up for approval in the next 45 days.
The Indian pharmaceutical industry is the 3rd
largest in the world by volume. It has high market presence in several advanced
economies such as the US and EU. The industry is well known for its production
of affordable medicines, particularly in the generics space. However the
country is significantly dependent on the import of basic raw materials, viz., Bulk Drugs that are used to
produce medicines.