Suppliers / Mepro Pharmaceuticals

Mepro Pharmaceuticals

India 485 employees Updated 9 July 2026

Mepro Pharmaceuticals is a finished-dose manufacturer based in India. It appears in 36 regulatory filings across 3 regulators, without an active US DMF or CEP on file. Its filings concentrate with DIGEMAPS (DO), MINSA (CR) and DAV (Vietnam). Its GMP standing is certified by EMA, CDSCO (India) and MHRA (UK). Customs aggregates show $30.5M of exports covering 1,294 molecules to 39 destinations in 2025.

0
active US DMFs
0
valid CEPs
5
registered plants
36
filings across 3 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
SURENDRANAGAR, India Not on file
Vadodra, India Not on file
Wadhwan City Surendra Nagar, India Not on file
surat 394 230surat, India Not on file
od samlaya roadvadodaravado dara 391 520, India Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
DIGEMAPS (DO) 28 None
MINSA (CR) 7 None
DAV (Vietnam) 1 None
EMA None 5
CDSCO (India) None 4
MHRA (UK) None 1

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $5.5M 24
2025 Not reported $30.5M 39
2024 Not reported $27.4M 43
2023 Not reported $22.7M 35

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 We do not publish the identity of any buyer.

Questions about Mepro Pharmaceuticals

Does Mepro Pharmaceuticals hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Mepro Pharmaceuticals. It does have 36 filings with 3 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Mepro Pharmaceuticals manufacture?
5 registered sites are on record, in India (Surendranagar, Vadodra and Wadhwan City Surendra Nagar among others). Every site is listed on this page with the register it came from.
Which regulators recognise Mepro Pharmaceuticals's GMP?
Current GMP certificates are on record from EMA, CDSCO (India) and MHRA (UK). 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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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