Suppliers / Marcyrl Pharmaceutical Industries

Marcyrl Pharmaceutical Industries

Egypt 2 duplicate records merged Updated 9 July 2026

Marcyrl Pharmaceutical Industries is a finished-dose manufacturer based in Egypt. It appears in 376 regulatory filings across 4 regulators, without an active US DMF or CEP on file. Its filings concentrate with EDA (EG), JFDA (JO) and UZPHARM (UZ). Its GMP standing is certified by EMA and TMDA (TZ).

0
active US DMFs
0
valid CEPs
2
registered plants
376
filings across 4 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
Cairo, Egypt Not on file
El Obour, Egypt Not on file

Filings and GMP by regulator

Regulator Filings GMP certificates
EDA (EG) 361 None
JFDA (JO) 9 None
UZPHARM (UZ) 5 None
MCAZ (ZW) 1 None
EMA None 3
TMDA (TZ) None 2

Questions about Marcyrl Pharmaceutical Industries

Does Marcyrl Pharmaceutical Industries hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Marcyrl Pharmaceutical Industries. It does have 376 filings with 4 regulators, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Marcyrl Pharmaceutical Industries manufacture?
2 registered sites are on record, in Egypt (Cairo and El Obour). Every site is listed on this page with the register it came from.
Which regulators recognise Marcyrl Pharmaceutical Industries'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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Sources on this page

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