Suppliers / Sohan Healthcare

Sohan Healthcare

India 3 duplicate records merged Updated 9 July 2026

Sohan Healthcare is an API manufacturer based in India. It holds one active US drug master file and 2 valid CEPs across a filed portfolio of 2 molecules. Its GMP standing is certified by EMA and CDSCO (India). Customs aggregates show $10.8M of exports covering 494 molecules to 43 destinations in 2025.

1
active US DMFs
2
valid CEPs
3
registered plants
3
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
Pune, India Not on file
Kurkumbh, India Not on file
Vadodara, India Not on file

What they file, and where

Molecule Regulators Docs
Metformin EDQM, US FDA 2
Gliclazide EDQM 1

Also appears on these molecule pages

Filings and GMP by regulator

Regulator Filings GMP certificates
BFARM (DE) 3 None
EMA None 4
CDSCO (India) None 2

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $1.4M 14
2025 Not reported $10.8M 43
2024 Not reported $20.5M 42
2023 Not reported $10.7M 41

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 We do not publish the identity of any buyer.

Questions about Sohan Healthcare

Does Sohan Healthcare hold a US DMF or a CEP?
Sohan Healthcare holds 1 active US drug master file and 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 Sohan Healthcare manufacture?
3 registered sites are on record, in India (Pune, Kurkumbh and Vadodara). Every site is listed on this page with the register it came from.
What does Sohan Healthcare make?
2 molecules are on record against Sohan Healthcare, including Metformin and Gliclazide. Each links through to that molecule's full manufacturer list.
Which regulators recognise Sohan Healthcare's GMP?
Current GMP certificates are on record from EMA and 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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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