Suppliers / Provepharm Sas

Provepharm Sas

France Updated 9 July 2026

Provepharm Sas is an API and finished-dose manufacturer based in France. It holds one active US drug master file. Its filings concentrate with EMA, US FDA and ANSM (FR). Its GMP standing is certified by ANSM (FR).

1
active US DMFs
0
valid CEPs
3
registered plants
46
filings across 12 regulators

Registered plants

Site FDA FEI
MARSEILLE, France Not on file
Marseille, France Not on file
Marseille, France Not on file

What they file, and where

Molecule Regulators Docs
Methylene Blue US FDA 1

Also appears on these molecule pages

Doxepin finished dose Methylene Blue API Piperacillin finished dose Tazobactam finished dose Tranexamic Acid finished dose

Filings and GMP by regulator

Regulator Filings GMP certificates
EMA 10 None
US FDA 9 None
ANSM (FR) 8 10
FAMHP (BE) 3 None
AEMPS (ES) 3 None
AIFA (IT) 3 None

Questions about Provepharm Sas

Does Provepharm Sas hold a US DMF or a CEP?
Provepharm Sas holds 1 active US drug master file. 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 Provepharm Sas manufacture?
3 registered sites are on record, in France (Marseille and Marseille among others). Every site is listed on this page with the register it came from.
What does Provepharm Sas make?
1 molecule is on record against Provepharm Sas, including Methylene Blue. Each links through to that molecule's full manufacturer list.
Which regulators recognise Provepharm Sas'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