Suppliers / Srs Pharmaceuticals

Srs Pharmaceuticals

India 29 employees Updated 9 July 2026

Srs Pharmaceuticals is a finished-dose manufacturer based in India. It appears in 38 regulatory filings across 6 regulators, without an active US DMF or CEP on file. Its filings concentrate with DAV (Vietnam), DIGEMAPS (DO) and MINSA (CR). Its GMP standing is certified by CDSCO (India). Customs aggregates show $6.9M of exports covering 181 molecules to 14 destinations in 2025.

0
active US DMFs
0
valid CEPs
3
registered plants
38
filings across 6 regulators

Registered plants

Site FDA FEI
tal dehgamzakgandhin agar, India Not on file
vado dara, India Not on file
navsari, India Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
DAV (Vietnam) 20 None
DIGEMAPS (DO) 9 None
MINSA (CR) 6 None
ARCSA (EC) 1 None
CDSCO (India) 1 4
UZPHARM (UZ) 1 None

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $178K 4
2025 Not reported $6.9M 14
2024 Not reported $5.8M 15
2023 Not reported $7.5M 18

Export figures are customs aggregates. We do not publish the identity of any buyer.

Questions about Srs Pharmaceuticals

Does Srs Pharmaceuticals hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Srs Pharmaceuticals. It does have 38 filings with 6 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Srs Pharmaceuticals manufacture?
3 registered sites are on record, in India (Tal Dehgamzakgandhin Agar, Vado Dara and Navsari). Every site is listed on this page with the register it came from.
Which regulators recognise Srs Pharmaceuticals's GMP?
Current GMP certificates are on record from CDSCO (India). GMP recognition covers the manufacturing site, separately from any filing on the substance itself.

Answered from this company's own record. Where a register holds nothing, the question is not asked rather than answered with a zero. How we count our figures.

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Ranked by shared active ingredients where we have them, otherwise by country and comparable credentials.

Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability
EudraGMDP and national regulators
GMP certificates
Customs aggregates
Export values, molecule and destination counts