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 US FDA and EMA. 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
Ambarnath, India Not on file
Thane, India 3010957801

What they file, and where

Molecule Regulators Docs
Metronidazole EDQM 1

Also appears on these molecule pages

Metronidazole API

Filings and GMP by regulator

Regulator Filings GMP certificates
US FDA None 1
EMA 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 We do not publish the identity of any buyer.

Questions about Acharya Chemicals

Does Acharya Chemicals hold a US DMF or a CEP?
Acharya Chemicals holds 1 valid CEP. 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.
Is Acharya Chemicals FDA-registered?
One site operated by Acharya Chemicals carries an FDA establishment identifier (FEI), which means it is registered with the FDA as a drug establishment. Registration is not the same as approval or inspection clearance.
How did Acharya Chemicals's last inspection go?
The most recent inspection on record closed on 15 March 2024 as VAI (Voluntary Action Indicated: issues were found but did not warrant regulatory action). 2 inspections are on file.
Where does Acharya Chemicals manufacture?
3 registered sites are on record, in India (Dombivli (east), Ambarnath and Thane). Every site is listed on this page with the register it came from.
What does Acharya Chemicals make?
1 molecule is on record against Acharya Chemicals, including Metronidazole. Each links through to that molecule's full manufacturer list.
Which regulators recognise Acharya Chemicals's GMP?
Current GMP certificates are on record from US FDA 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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Open risk flags

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

Comparable suppliers

Unichem Laboratories shares 1 molecule Wuhan Wuyao Pharmaceutical shares 1 molecule Bajaj Healthcare shares 1 molecule Hubei Hongyuan Pharmaceutical Technology shares 1 molecule Imexpharm 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