Suppliers / Aristopharma

Aristopharma

Bangladesh 762 employees Updated 9 July 2026

Aristopharma is a finished-dose manufacturer based in Bangladesh. It appears in 65 regulatory filings across 5 regulators, without an active US DMF or CEP on file. Its filings concentrate with DAV (Vietnam), NAFDAC (NG) and DIGEMAPS (DO). Its GMP standing is certified by NAFDAC (NG), FDA (GH) and EMA.

0
active US DMFs
0
valid CEPs
2
registered plants
65
filings across 5 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
Gazipur, Bangladesh Not on file
DHAKA, Nigeria Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
DAV (Vietnam) 26 None
NAFDAC (NG) 19 2
DIGEMAPS (DO) 10 None
FDA (GH) 9 1
BOMRA (BW) 1 None
EMA None 1

Questions about Aristopharma

Does Aristopharma hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Aristopharma. It does have 65 filings with 5 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Aristopharma manufacture?
2 registered sites are on record, in Bangladesh and Nigeria (Gazipur and Dhaka). Every site is listed on this page with the register it came from.
Which regulators recognise Aristopharma's GMP?
Current GMP certificates are on record from NAFDAC (NG), FDA (GH) 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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Comparable suppliers

ACME Laboratories also in Bangladesh Beximco Pharmaceuticals also in Bangladesh Eskayef Pharmaceuticals also in Bangladesh General Pharmaceuticals also in Bangladesh Incepta Pharmaceuticals also in Bangladesh

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