Suppliers / Acme Generics

Acme Generics

India Updated 9 July 2026

Acme Generics is a finished-dose manufacturer based in India. It appears in 46 regulatory filings across 7 regulators, without an active US DMF or CEP on file. Its filings concentrate with ARCSA (EC), DAV (Vietnam) and BOMRA (BW). Its GMP standing is certified by EMA, ANVISA (Brazil) and FDA (GH). Customs aggregates show $18.3M of exports covering 527 molecules to 19 destinations in 2025.

0
active US DMFs
0
valid CEPs
3
registered plants 1 with an FDA FEI number
46
filings across 7 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
1 of 1 confirmed
EU GMP
1 of 1 confirmed
Sources: FDA Establishment Registration, read 4 May 2026. EudraGMDP (MIA + third-country GMP certs), read 4 May 2026.

Registered plants

Site FDA FEI
Solan, India 3012112224
HIMACHAL PRADESH, India Not on file
Guru Majra, India Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
ARCSA (EC) 14 None
DAV (Vietnam) 11 None
BOMRA (BW) 5 None
DIGEMAPS (DO) 5 None
CDSCO (India) 5 None
NCELS (KZ) 4 None
EMA None 4
ANVISA (Brazil) None 1
FDA (GH) None 1

Scale

Year Revenue Exports Destinations
2026 YTD Not reported $1.9M 8
2025 Not reported $18.3M 19
2024 Not reported $8.6M 18
2023 Not reported $5.9M 12

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 We do not publish the identity of any buyer.

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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