Suppliers / Anuh Pharma

Anuh Pharma

India 153 employees Updated 9 July 2026

Anuh Pharma is an API manufacturer based in India. It holds 3 valid CEPs across a filed portfolio of 4 molecules. Its GMP standing is certified by US FDA and EMA. Its most recent recorded inspection, by US FDA, closed on 6 February 2026 as NAI. Customs aggregates show $42.1M of exports covering 957 molecules to 78 destinations in 2025.

0
active US DMFs
3
valid CEPs
3
registered plants 1 with an FDA FEI number
5
filings across 1 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

  • 6 February 2026 NAI US FDA
  • 20 September 2019 NAI US FDA

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

Registered plants

Site FDA FEI
Mumbai, India Not on file
Thane, India 3001174909
Boisar, India Not on file

What they file, and where

Molecule Regulators Docs
Betamethasone SFDA (Saudi Arabia) 1
Pyrazinamide EDQM 1
Sulfadimethoxine EDQM 1
Sulfadoxine EDQM 1

Also appears on these molecule pages

Filings and GMP by regulator

Regulator Filings GMP certificates
MINSA (CR) 5 None
US FDA None 1
EMA None 1

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $5.1M 38
2025 Not reported $42.1M 78
2024 Not reported $28.0M 69
2023 Not reported $30.2M 65

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 We do not publish the identity of any buyer.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 NAI, on 6 February 2026.

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