Suppliers / Acharya Chemicals

Acharya Chemicals

India Updated 9 July 2026

Acharya Chemicals is an API manufacturer based in India. It holds one valid CEP. Its GMP standing is certified by EMA and US FDA. Its most recent recorded inspection, by US FDA, closed on 15 March 2024 as VAI. Customs aggregates show $860K of exports covering 15 molecules to 6 destinations in 2025.

0
active US DMFs
1
valid CEPs
3
registered plants 1 with an FDA FEI number
0
filings across 0 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
1 of 1 confirmed
Inspections
2 of 2 confirmed
EU GMP
1 of 1 confirmed
Sources: FDA Establishment Registration, read 4 May 2026. FDA drug inspection classifications, read 4 May 2026. EudraGMDP (MIA + third-country GMP certs), read 4 May 2026.

Inspection history

  • 15 March 2024 VAI US FDA
  • 24 June 2016 VAI US FDA

NAI means no action indicated, VAI means voluntary action indicated, and OAI means official action indicated.

Registered plants

Site FDA FEI
Dombivli (East), India Not on file
Thane, India 3010957801
Ambarnath, India Not on file

What they file, and where

Molecule Regulators Docs
Metronidazole EDQM 1

Also appears on these molecule pages

Filings and GMP by regulator

Regulator Filings GMP certificates
EMA None 1
US FDA None 1

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $460K 3
2025 Not reported $860K 6
2024 Not reported $993K 6
2023 Not reported $514K 4

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 We do not publish the identity of any buyer.

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Open risk flags

  • The most recent inspection outcome was VAI, on 15 March 2024.

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