Suppliers / CF Pharma

CF Pharma

Hungary reconciled across 6 public records · 3 entities Updated 9 July 2026

CF Pharma is an API manufacturer based in Hungary. It holds 5 active US drug master files and 6 valid CEPs across a filed portfolio of 8 molecules. Its GMP standing is certified by COFEPRIS (MX).

5
active US DMFs
6
valid CEPs
3
registered plants
0
filings across 0 regulators

Registered plants

Site FDA FEI
KFT. Budapest IX, Hungary Not on file
Budapest, Hungary Not on file
Textil de Juárez, Mexico Not on file

What they file, and where

Molecule Regulators Docs
Cisatracurium EDQM, SFDA (Saudi Arabia), US FDA 5
Atracurium Besylate EDQM, SFDA (Saudi Arabia) 2
Biperiden Hydrochloride EDQM 2
Methotrexate EDQM, US FDA 2
Atracurium Besilate EDQM 1
Bicalutamide SFDA (Saudi Arabia) 1
Biperiden EDQM 1
Cabergoline US FDA 1

Also appears on these molecule pages

Filings and GMP by regulator

Regulator Filings GMP certificates
COFEPRIS (MX) None 2

Questions about CF Pharma

Does CF Pharma hold a US DMF or a CEP?
CF Pharma holds 5 active US drug master files and 6 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 CF Pharma manufacture?
3 registered sites are on record, in Hungary and Mexico (Kft. Budapest IX, Budapest and Textil De Juárez). Every site is listed on this page with the register it came from.
What does CF Pharma make?
8 molecules are on record against CF Pharma, including Cisatracurium, Atracurium Besylate, Biperiden Hydrochloride and Methotrexate. Each links through to that molecule's full manufacturer list.
Which regulators recognise CF Pharma's GMP?
Current GMP certificates are on record from COFEPRIS (MX). 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