Sanofi

Egypt Updated 9 July 2026

Sanofi is an API manufacturer based in Egypt. It appears in 595 regulatory filings across 6 regulators, without an active US DMF or CEP on file. Its filings concentrate with MHRA (UK), EDA (EG) and DKMA (DK).

active US DMFs

valid CEPs

registered plants

595

filings across 6 regulators

What they file, and where

Molecule	Regulators	Docs
Acetylcysteine	DAV (Vietnam)	1
Cetirizine	DAV (Vietnam)	1
Clotrimazole	DAV (Vietnam)	1
Lactoserum Atomisắt	DAV (Vietnam)	1

Also appears on these molecule pages

Acetylcysteine API Cetirizine API Clotrimazole API

Filings and GMP by regulator

Regulator	Filings	GMP certificates
MHRA (UK)	376	None
EDA (EG)	132	None
DKMA (DK)	64	None
DMP (NO)	18	None
RAMA (GE)	3	None
DPM (TN)	2	None

Questions about Sanofi

Does Sanofi hold a US DMF or a CEP?

No active US drug master file or valid CEP is on record for Sanofi. It does have 595 filings with 6 regulators, so it is registered, just not with the two strong registers buyers usually screen on.

What does Sanofi make?

4 molecules are on record against Sanofi, including Acetylcysteine, Cetirizine, Clotrimazole and Lactoserum Atomisắt. Each links through to that molecule's full manufacturer list.

Where does Sanofi file?

Filings are on record with MHRA (UK), EDA (EG), DKMA (DK), DMP (NO) and 2 other regulators, 595 in total.

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

F.I.S. Fabbrica Italiana Sintetici shares 2 molecules Imexpharm shares 2 molecules Cipla shares 1 molecule Dr Reddy's Laboratories shares 1 molecule Olon shares 1 molecule

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