Suppliers / Amsal Chem

Amsal Chem

India 20 employees 2 duplicate records merged Updated 9 July 2026

Amsal Chem is an API manufacturer based in India. Its GMP standing is certified by CDSCO (India) and EMA. Customs aggregates show $901K of exports covering 71 molecules to 26 destinations in 2025.

0
active US DMFs
0
valid CEPs
2
registered plants
0
filings across 0 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
at post ankleshwarbharuc h, India Not on file
Ankleshwar, India Not on file

What they file, and where

Molecule Regulators Docs
Isoniazid SFDA (Saudi Arabia) 1

Also appears on these molecule pages

Isoniazid API

Filings and GMP by regulator

Regulator Filings GMP certificates
CDSCO (India) None 2
EMA None 1

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $815K 29
2025 Not reported $901K 26

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 We do not publish the identity of any buyer.

Questions about Amsal Chem

Where does Amsal Chem manufacture?
2 registered sites are on record, in India (At Post Ankleshwarbharuc H and Ankleshwar). Every site is listed on this page with the register it came from.
What does Amsal Chem make?
1 molecule is on record against Amsal Chem, including Isoniazid. Each links through to that molecule's full manufacturer list.
Which regulators recognise Amsal Chem's GMP?
Current GMP certificates are on record from CDSCO (India) and EMA. 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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Comparable suppliers

Calyx Chemicals and Pharmaceuticals shares 1 molecule Chongqing Huapont Shengchem Pharmaceutical shares 1 molecule Yuki Gosei Kogyo shares 1 molecule Yangzhou Pharmaceutical shares 1 molecule

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