Suppliers / Francopia A Euroapi

Francopia A Euroapi

France Updated 9 July 2026

The public registers hold a second record for Francopia A Euroapi. The fuller profile, with 48 active US DMFs and 53 valid CEPs, is at EUROAPI. Figures on this page cover only this record.

Francopia A Euroapi is an API manufacturer based in France. It holds 4 active US drug master files across a filed portfolio of 4 molecules.

4
active US DMFs
0
valid CEPs
0
registered plants
0
filings across 0 regulators

What they file, and where

Molecule Regulators Docs
Apomorphine US FDA 1
Nalbuphine US FDA 1
Naloxone US FDA 1
Naltrexone US FDA 1

Also appears on these molecule pages

Naloxone API Naltrexone API

Questions about Francopia A Euroapi

Does Francopia A Euroapi hold a US DMF or a CEP?
Francopia A Euroapi holds 4 active US drug master files. 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.
What does Francopia A Euroapi make?
4 molecules are on record against Francopia A Euroapi, including Apomorphine, Nalbuphine, Naloxone and Naltrexone. Each links through to that molecule's full manufacturer list.

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