Suppliers / General Pharmaceuticals

General Pharmaceuticals

Bangladesh 787 employees 3 duplicate records merged Updated 9 July 2026

General Pharmaceuticals is a finished-dose manufacturer based in Bangladesh. It appears in 20 regulatory filings across 5 regulators, without an active US DMF or CEP on file. Its filings concentrate with ARCSA (EC), EFDA (ET) and DAV (Vietnam). Its GMP standing is certified by EMA and TMDA (TZ).

0
active US DMFs
0
valid CEPs
1
registered plants
20
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

Filings and GMP by regulator

Regulator Filings GMP certificates
ARCSA (EC) 6 None
EFDA (ET) 6 None
DAV (Vietnam) 4 None
DIGEMAPS (DO) 3 None
MINSA (CR) 1 None
EMA None 1
TMDA (TZ) None 1

Questions about General Pharmaceuticals

Does General Pharmaceuticals hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for General Pharmaceuticals. It does have 20 filings with 5 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does General Pharmaceuticals manufacture?
1 registered site is on record, in Bangladesh (Gazipur). Every site is listed on this page with the register it came from.
Which regulators recognise General Pharmaceuticals's GMP?
Current GMP certificates are on record from EMA and TMDA (TZ). 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 Aristopharma also in Bangladesh Beximco Pharmaceuticals also in Bangladesh Eskayef 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