Suppliers / Nouryon Chemicals, S.A. de C.V

Nouryon Chemicals, S.A. de C.V

Mexico Updated 9 July 2026

Nouryon Chemicals, S.A. de C.V is an API manufacturer based in Mexico. It holds one valid CEP across a filed portfolio of 2 molecules. Its GMP standing is certified by COFEPRIS (MX) and US FDA. Its most recent recorded inspection, by US FDA, closed on 10 November 2023 as VAI.

0
active US DMFs
1
valid CEPs
3
registered plants 1 with an FDA FEI number
0
filings across 0 regulators
These figures were checked against the regulators' own files on 25 July 2026
Plants
1 of 1 confirmed
Inspections
3 of 3 confirmed
Sources: FDA Establishment Registration, read 4 May 2026. FDA drug inspection classifications, read 4 May 2026.

Inspection history

  • 10 November 2023 VAI US FDA
  • 13 February 2015 VAI US FDA
  • 30 March 2012 VAI US FDA

NAI means no action indicated, VAI means voluntary action indicated, and OAI means official action indicated.

Registered plants

Site FDA FEI
S.A. DE C.V Tecamachalco, Mexico Not on file
Los Reyes la Paz, Mexico Not on file
Mexico, Mexico 3003882630

What they file, and where

Molecule Regulators Docs
Benzoyl Peroxide EDQM 1
Hydrous Benzoyl Peroxide SFDA (Saudi Arabia) 1

Also appears on these molecule pages

Benzoyl Peroxide API

Filings and GMP by regulator

Regulator Filings GMP certificates
COFEPRIS (MX) None 2
US FDA None 1

Questions about Nouryon Chemicals, S.A. de C.V

Does Nouryon Chemicals, S.A. de C.V hold a US DMF or a CEP?
Nouryon Chemicals, S.A. de C.V holds 1 valid CEP. 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.
Is Nouryon Chemicals, S.A. de C.V FDA-registered?
One site operated by Nouryon Chemicals, S.A. de C.V carries an FDA establishment identifier (FEI), which means it is registered with the FDA as a drug establishment. Registration is not the same as approval or inspection clearance.
How did Nouryon Chemicals, S.A. de C.V's last inspection go?
The most recent inspection on record closed on 10 November 2023 as VAI (Voluntary Action Indicated: issues were found but did not warrant regulatory action). 3 inspections are on file.
Where does Nouryon Chemicals, S.A. de C.V manufacture?
3 registered sites are on record, in Mexico (S.a. DE C.v Tecamachalco, Los Reyes La Paz and Mexico). Every site is listed on this page with the register it came from.
What does Nouryon Chemicals, S.A. de C.V make?
2 molecules are on record against Nouryon Chemicals, S.A. de C.V, including Benzoyl Peroxide and Hydrous Benzoyl Peroxide. Each links through to that molecule's full manufacturer list.
Which regulators recognise Nouryon Chemicals, S.A. de C.V's GMP?
Current GMP certificates are on record from COFEPRIS (MX) and US FDA. 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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Open risk flags

  • The most recent inspection outcome was VAI, on 10 November 2023.

Comparable suppliers

Zydus Lifesciences shares 1 molecule Cambrex Karlskoga AB shares 1 molecule Fermic Sa De Cv also in Mexico Sintenovo SA de CV also in Mexico Abbott Laboratories De México, S. A. De C. V also in Mexico

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