Suppliers / Chemino Pharma

Chemino Pharma

India 29 employees Updated 9 July 2026

Chemino Pharma is an API manufacturer based in India. It holds 2 valid CEPs across a filed portfolio of 2 molecules. Its GMP standing is certified by CDSCO (India). Customs aggregates show $178K of exports covering 23 molecules to 6 destinations in 2025.

0
active US DMFs
2
valid CEPs
3
registered plants
0
filings across 0 regulators

Registered plants

Site FDA FEI
Mumbai, India Not on file
valsad 396 195, India Not on file
Valsad, India Not on file

What they file, and where

Molecule Regulators Docs
Fenbendazole For Veterinary Use EDQM 1
Lidocaine EDQM 1

Also appears on these molecule pages

Lidocaine API

Filings and GMP by regulator

Regulator Filings GMP certificates
CDSCO (India) None 2

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $16K 3
2025 Not reported $178K 6
2024 Not reported $147K 7
2023 Not reported $112K 6

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 We do not publish the identity of any buyer.

Questions about Chemino Pharma

Does Chemino Pharma hold a US DMF or a CEP?
Chemino Pharma holds 2 valid CEPs. A drug master file is a submission to the FDA describing how an ingredient is made; a CEP is the EDQM's certificate that the substance meets its European Pharmacopoeia monograph. Both are filings rather than approvals.
Where does Chemino Pharma manufacture?
3 registered sites are on record, in India (Mumbai, Valsad 396 195 and Valsad). Every site is listed on this page with the register it came from.
What does Chemino Pharma make?
2 molecules are on record against Chemino Pharma, including Fenbendazole For Veterinary Use and Lidocaine. Each links through to that molecule's full manufacturer list.
Which regulators recognise Chemino Pharma'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