Suppliers / Signa Sa De Cv

Signa Sa De Cv

Mexico Updated 9 July 2026

Signa Sa De Cv is an API manufacturer based in Mexico. It holds 16 active US drug master files across a filed portfolio of 16 molecules.

16
active US DMFs
0
valid CEPs
0
registered plants
0
filings across 0 regulators

What they file, and where

Molecule Regulators Docs
Clopidogrel US FDA 2
Acyclovir US FDA 1
Allopurinol US FDA 1
Atorvastatin Calcium Propylene Glycol Solvate SFDA (Saudi Arabia) 1
Balsalazide US FDA 1
Duloxetine US FDA 1
Famciclovir US FDA 1
Fesoterodine US FDA 1
Lacosamide US FDA 1
Lamivudine US FDA 1
Show all 16 molecules on file
Nadolol US FDA 1
Oxcarbazepine US FDA 1
Paroxetine US FDA 1
Pirfenidone US FDA 1
Sitagliptin US FDA 1
Terazosin US FDA 1

Also appears on these molecule pages

Allopurinol API Famciclovir API Fesoterodine API Lamivudine API Nadolol API Oxcarbazepine API Paroxetine API Terazosin API Clopidogrel API Sitagliptin API Acyclovir API Duloxetine API
Show 2 more molecule pages
Lacosamide API Pirfenidone API

Questions about Signa Sa De Cv

Does Signa Sa De Cv hold a US DMF or a CEP?
Signa Sa De Cv holds 16 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 Signa Sa De Cv make?
16 molecules are on record against Signa Sa De Cv, including Clopidogrel, Acyclovir, Allopurinol and Atorvastatin Calcium Propylene Glycol Solvate. 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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Comparable suppliers

Apitoria Pharma shares 4 molecules Hetero shares 4 molecules Matrix Pharmacorp shares 4 molecules Jubilant Biosys shares 3 molecules Cipla shares 2 molecules

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