Suppliers / Incepta Pharmaceuticals

Incepta Pharmaceuticals

Bangladesh 2 employees 3 duplicate records merged Updated 9 July 2026

Incepta Pharmaceuticals is a finished-dose manufacturer based in Bangladesh. It appears in 36 regulatory filings across 8 regulators, without an active US DMF or CEP on file. Its filings concentrate with DIGEMAPS (DO), NAFDAC (NG) and MINSA (CR). Its GMP standing is certified by EMA, NAFDAC (NG) and TMDA (TZ).

0
active US DMFs
0
valid CEPs
3
registered plants
36
filings across 8 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
Dhaka, United Arab Emirates Not on file
Dhaka, Bangladesh Not on file
DHAKA, Nigeria Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
DIGEMAPS (DO) 9 None
NAFDAC (NG) 7 2
MINSA (CR) 7 None
ARCSA (EC) 6 None
UZPHARM (UZ) 3 None
TMDA (TZ) 2 1
EMA None 2

Questions about Incepta Pharmaceuticals

Does Incepta Pharmaceuticals hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Incepta Pharmaceuticals. It does have 36 filings with 8 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Incepta Pharmaceuticals manufacture?
3 registered sites are on record, in United Arab Emirates, Bangladesh and Nigeria (Dhaka and Dhaka among others). Every site is listed on this page with the register it came from.
Which regulators recognise Incepta Pharmaceuticals's GMP?
Current GMP certificates are on record from EMA, NAFDAC (NG) 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.

Comparing suppliers?

Choose your molecules and target markets. Incepta Pharmaceuticals comes back tiered against every other supplier able to file there.

Start for free
No sales call.

Sources on this page

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