Suppliers / Interquim Sa De Cv

Interquim Sa De Cv

Mexico Updated 9 July 2026

The public registers hold a second record for Interquim Sa De Cv. The fuller profile, with 24 active US DMFs and 0 valid CEPs, is at Interquim. Figures on this page cover only this record.

Interquim Sa De Cv is an API manufacturer based in Mexico. 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
Dexmedetomidine US FDA 1
Fosfomycin US FDA 1
Pyrimethamine US FDA 1
Tiamulin US FDA 1

Also appears on these molecule pages

Dexmedetomidine API Fosfomycin API

Questions about Interquim Sa De Cv

Does Interquim Sa De Cv hold a US DMF or a CEP?
Interquim Sa De Cv 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 Interquim Sa De Cv make?
4 molecules are on record against Interquim Sa De Cv, including Dexmedetomidine, Fosfomycin, Pyrimethamine and Tiamulin. 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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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