Suppliers / Suven Pharmaceuticals

Suven Pharmaceuticals

India 261 employees 2 duplicate records merged Updated 9 July 2026

Suven Pharmaceuticals is an API manufacturer based in India. It holds 20 active US drug master files across a filed portfolio of 9 molecules. Its GMP standing is certified by EMA. Customs aggregates show $42.0M of exports covering 153 molecules to 27 destinations in 2025.

20
active US DMFs
0
valid CEPs
1
registered plants
1
filings across 1 regulators
These figures were checked against the regulators' own files on 25 July 2026
EU GMP
1 of 1 confirmed
Sources: EudraGMDP (MIA + third-country GMP certs), read 4 May 2026.

Registered plants

Site FDA FEI
Sangareddy, India Not on file

What they file, and where

Molecule Regulators Docs
Entacapone US FDA 4
Danofloxacin US FDA 2
Doxofylline US FDA 2
Fenoprofen US FDA 2
Gabapentin US FDA 2
Glycopyrronium US FDA 2
Iron Sucrose US FDA 2
Isosulfan Blue US FDA 2
Metyrosine US FDA 2

Also appears on these molecule pages

Filings and GMP by regulator

Regulator Filings GMP certificates
CDSCO (India) 1 None
EMA None 1

Scale

Year Revenue Exports Destinations
2025 Not reported $42.0M 27
2024 Not reported $95.3M 24
2023 Not reported $112.0M 26
2022 Not reported $162.9M 26

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 We do not publish the identity of any buyer.

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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