Suppliers / Uquifa

Uquifa

Italy reconciled across 9 public records · 2 entities Updated 9 July 2026

Uquifa is an API manufacturer based in Italy. It holds 5 active US drug master files across a filed portfolio of 6 molecules. Its GMP standing is certified by COFEPRIS (MX).

5
active US DMFs
0
valid CEPs
1
registered plants
0
filings across 0 regulators

Registered plants

Site FDA FEI
Jiutepec, Mexico Not on file

What they file, and where

Molecule Regulators Docs
Pyrantel US FDA 4
Carisoprodol US FDA 1
Ciprofloxacin SFDA (Saudi Arabia) 1
Cyclopentolate SFDA (Saudi Arabia) 1
Esomeprazole SFDA (Saudi Arabia) 1
Quetiapine SFDA (Saudi Arabia) 1

Also appears on these molecule pages

Carisoprodol API Pyrantel API

Filings and GMP by regulator

Regulator Filings GMP certificates
COFEPRIS (MX) None 2

Questions about Uquifa

Does Uquifa hold a US DMF or a CEP?
Uquifa holds 5 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.
Where does Uquifa manufacture?
1 registered site is on record, in Mexico (Jiutepec). Every site is listed on this page with the register it came from.
What does Uquifa make?
6 molecules are on record against Uquifa, including Pyrantel, Carisoprodol, Ciprofloxacin and Cyclopentolate. Each links through to that molecule's full manufacturer list.
Which regulators recognise Uquifa'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