Suppliers / Eskayef Pharmaceuticals

Eskayef Pharmaceuticals

Bangladesh Updated 9 July 2026

Eskayef Pharmaceuticals is a finished-dose manufacturer based in Bangladesh. It appears in 29 regulatory filings across 5 regulators, without an active US DMF or CEP on file. Its filings concentrate with TMDA (TZ), DIGEMAPS (DO) and UZPHARM (UZ). Its GMP standing is certified by UZPHARM (UZ), MHRA (UK) and ANVISA (Brazil), among 4 authorities.

0
active US DMFs
0
valid CEPs
3
registered plants 1 with an FDA FEI number
29
filings across 5 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
1 of 1 confirmed
Sources: FDA Establishment Registration, read 4 May 2026.

Registered plants

Site FDA FEI
GAZIPUR, Bangladesh Not on file
TONGI, Bangladesh Not on file
Bangladesh, Bangladesh 3014835149

Filings and GMP by regulator

Regulator Filings GMP certificates
TMDA (TZ) 10 1
DIGEMAPS (DO) 7 None
UZPHARM (UZ) 7 2
US FDA 4 None
BOMRA (BW) 1 None
MHRA (UK) None 2
ANVISA (Brazil) None 1

Questions about Eskayef Pharmaceuticals

Does Eskayef Pharmaceuticals hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Eskayef Pharmaceuticals. It does have 29 filings with 5 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Is Eskayef Pharmaceuticals FDA-registered?
One site operated by Eskayef Pharmaceuticals carries an FDA establishment identifier (FEI), which means it is registered with the FDA as a drug establishment. Registration is not the same as approval or inspection clearance.
Where does Eskayef Pharmaceuticals manufacture?
3 registered sites are on record, in Bangladesh (Gazipur, Tongi and Bangladesh). Every site is listed on this page with the register it came from.
Which regulators recognise Eskayef Pharmaceuticals's GMP?
Current GMP certificates are on record from UZPHARM (UZ), MHRA (UK), ANVISA (Brazil) 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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Sources on this page

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