Suppliers / Sicor Societá Italiana C

Sicor Societá Italiana C

Italy Updated 9 July 2026

Sicor Societá Italiana C is an API manufacturer based in Italy. It appears in 1 regulatory filing across 1 regulator, without an active US DMF or CEP on file. Its GMP standing is certified by COFEPRIS (MX).

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

Registered plants

Site FDA FEI
Lerma, Mexico Not on file

What they file, and where

Molecule Regulators Docs
Rocuronium SFDA (Saudi Arabia) 2
Albuterol SFDA (Saudi Arabia) 1
Bleomycin SFDA (Saudi Arabia) 1
Cisatracurium SFDA (Saudi Arabia) 1
Fluocinolone Acetonide SFDA (Saudi Arabia) 1
Haloperidol Decanoate SFDA (Saudi Arabia) 1

Also appears on these molecule pages

Albuterol API Cisatracurium API Fluocinolone Acetonide API Haloperidol Decanoate API Rocuronium API Salbutamol API

Filings and GMP by regulator

Regulator Filings GMP certificates
MINSA (CR) 1 None
COFEPRIS (MX) None 2

Questions about Sicor Societá Italiana C

Does Sicor Societá Italiana C hold a US DMF or a CEP?
No active US drug master file or valid CEP is on record for Sicor Societá Italiana C. It does have 1 filing with one regulator, so it is registered, just not with the two strong registers buyers usually screen on.
Where does Sicor Societá Italiana C manufacture?
1 registered site is on record, in Mexico (Lerma). Every site is listed on this page with the register it came from.
What does Sicor Societá Italiana C make?
6 molecules are on record against Sicor Societá Italiana C, including Rocuronium, Albuterol, Bleomycin and Cisatracurium. Each links through to that molecule's full manufacturer list.
Which regulators recognise Sicor Societá Italiana C'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