Suppliers / Sanofi Chimie

Sanofi Chimie

France Updated 9 July 2026

Sanofi Chimie is an API manufacturer based in France. It holds 2 valid CEPs across a filed portfolio of 9 molecules. Its GMP standing is certified by ANSM (FR).

0
active US DMFs
2
valid CEPs
12
registered plants
1
filings across 1 regulators

Registered plants

Site FDA FEI
PLOERMEL, France Not on file
NEUVILLE SUR SAONE, France Not on file
VERTOLAYE, France Not on file
VITRY-SUR-SEINE, France Not on file
SISTERON CEDEX, France Not on file
SAINT AUBIN LES ELBEUF, France Not on file

6 further sites are on record.

What they file, and where

Molecule Regulators Docs
Apomorphine SFDA (Saudi Arabia) 1
Cyanocobalamin SFDA (Saudi Arabia) 1
Docetaxel SFDA (Saudi Arabia) 1
Heptaminol EDQM 1
Morphine SFDA (Saudi Arabia) 1
Nalbuphine SFDA (Saudi Arabia) 1
Naloxone SFDA (Saudi Arabia) 1
Prednisolone SFDA (Saudi Arabia) 1
Tiapride EDQM 1

Also appears on these molecule pages

Morphine API Naloxone API Prednisolone API Docetaxel API

Filings and GMP by regulator

Regulator Filings GMP certificates
INVIMA (CO) 1 None
ANSM (FR) None 162

Questions about Sanofi Chimie

Does Sanofi Chimie hold a US DMF or a CEP?
Sanofi Chimie holds 2 valid CEPs. A drug master file is a submission to the FDA describing how an ingredient is made; a CEP is the EDQM's certificate that the substance meets its European Pharmacopoeia monograph. Both are filings rather than approvals.
Where does Sanofi Chimie manufacture?
12 registered sites are on record, in France (Ploermel, Neuville SUR Saone and Vertolaye among others). Every site is listed on this page with the register it came from.
What does Sanofi Chimie make?
9 molecules are on record against Sanofi Chimie, including Apomorphine, Cyanocobalamin, Docetaxel and Heptaminol. Each links through to that molecule's full manufacturer list.
Which regulators recognise Sanofi Chimie's GMP?
Current GMP certificates are on record from ANSM (FR). 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