Suppliers / Akums Drugs & Pharmaceuticals

Akums Drugs & Pharmaceuticals

India Updated 9 July 2026

Akums Drugs & Pharmaceuticals is a finished-dose manufacturer based in India. It appears in 222 regulatory filings across 10 regulators, without an active US DMF or CEP on file. Its filings concentrate with CDSCO (India), DAV (Vietnam) and NAFDAC (NG). Its GMP standing is certified by NAFDAC (NG), CDSCO (India) and EMA, among 5 authorities.

0
active US DMFs
0
valid CEPs
7
registered plants
222
filings across 10 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
HARIDWAR, India Not on file
Haridwar-249403, India Not on file
Haridwar, India Not on file
Haridwar, Nigeria Not on file
Haridwar, Nigeria Not on file
Haridwar, Nigeria Not on file

1 further sites are on record.

Filings and GMP by regulator

Regulator Filings GMP certificates
CDSCO (India) 123 4
DAV (Vietnam) 46 None
NAFDAC (NG) 22 5
UZPHARM (UZ) 16 None
DIGEMAPS (DO) 5 None
MINSA (CR) 5 None
EMA None 4
FDA (GH) None 2
ANVISA (Brazil) None 1

Questions about Akums Drugs & Pharmaceuticals

Does Akums Drugs & Pharmaceuticals hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Akums Drugs & Pharmaceuticals. It does have 222 filings with 10 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Akums Drugs & Pharmaceuticals manufacture?
7 registered sites are on record, in India and Nigeria (Haridwar, Haridwar-249403 and Haridwar among others). Every site is listed on this page with the register it came from.
Which regulators recognise Akums Drugs & Pharmaceuticals's GMP?
Current GMP certificates are on record from NAFDAC (NG), CDSCO (India), EMA, FDA (GH) and ANVISA (Brazil). 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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Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability
EudraGMDP and national regulators
GMP certificates