Suppliers / UQUIFA Mexico, S.A. DE C.V

UQUIFA Mexico, S.A. DE C.V

Mexico Updated 9 July 2026

The public registers hold a second record for UQUIFA Mexico, S.A. DE C.V. The fuller profile, with 5 active US DMFs and 0 valid CEPs, is at Uquifa. Figures on this page cover only this record.

UQUIFA Mexico, S.A. DE C.V is an API manufacturer based in Mexico. Its GMP standing is certified by COFEPRIS (MX).

0
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
Ciprofloxacin SFDA (Saudi Arabia) 1
Cyclopentolate SFDA (Saudi Arabia) 1
Quetiapine SFDA (Saudi Arabia) 1

Also appears on these molecule pages

Ciprofloxacin API Quetiapine API

Filings and GMP by regulator

Regulator Filings GMP certificates
COFEPRIS (MX) None 2

Questions about UQUIFA Mexico, S.A. DE C.V

Where does UQUIFA Mexico, S.A. DE C.V 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 Mexico, S.A. DE C.V make?
3 molecules are on record against UQUIFA Mexico, S.A. DE C.V, including Ciprofloxacin, Cyclopentolate and Quetiapine. Each links through to that molecule's full manufacturer list.
Which regulators recognise UQUIFA Mexico, S.A. DE C.V'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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Ranked by shared active ingredients where we have them, otherwise by country and comparable credentials.

Sources on this page

FDA
Drug master files, establishment registration, inspection classifications
EDQM
Certificates of suitability
EudraGMDP and national regulators
GMP certificates