Is Signa S.A. de C.V. FDA approved?

Signa S.A. de C.V. holds 1 FDA-registered establishment in Mexico. Registration puts a site on the FDA's register and open to inspection; it is not an approval of the company. Approvals attach to individual drug applications.

Where are Signa S.A. de C.V.'s drugs manufactured?

The FDA register lists Toluca. Registered operations: analytical testing, active ingredient (API) manufacture.

What drugs does Signa S.A. de C.V. make?

9 products are listed under Signa S.A. de C.V. in the openFDA NDC Directory, most often as powder. The full breakdown by dosage form and route is above. A listing count is not a sales figure.

Signa S.A. de C.V.

Data as of 24 Sept 2026 · How to read this entry

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Registered sites: 1
Active NDC listings: 9
Live patents: 0
Countries: 1
Base: Mexico

Authorisation

Registered operations

Analytical testing1Active ingredient (API) manufacture1

Sites

Registered establishments

Establishment	Address	Registered for	FEI / DUNS
Signa S.A. de C.V.	Av. Industria Automotriz No. 301, Zona Industrial Toluca, Toluca, Estado de Mexico CP. 50071, Mexico (MEX)	Analytical testing, Active ingredient (API) manufacture	3002808161810419275

Catalogue

Drug listings by form and route

9 active NDC listings: 9 bulk ingredient. By marketing category: BULK INGREDIENT 9.

Dosage form	NDCs
powder	9

Route	NDCs

Labeller name on the listing	NDCs
signa s.a. de c.v.	9

Catalogue

Marketed products

Brand	Generic name	Form / route	NDC
-	ACYCLOVIR	powder	50787-0037BULK INGREDIENT
-	ATORVASTATIN CALCIUM PROPYLENE GLYCOL SOLVATE	powder	50787-0059BULK INGREDIENT
-	BALSALAZIDE	powder	50787-0032BULK INGREDIENT
-	CLOPIDOGREL	powder	50787-0022BULK INGREDIENT
-	DULOXETINE HYDROCHLORIDE	powder	50787-0040BULK INGREDIENT
-	FAMCICLOVIR	powder	50787-0016BULK INGREDIENT
-	LAMIVUDINE	powder	50787-0027BULK INGREDIENT
-	PAROXETINE HYDROCHLORIDE HEMIHYDRATE	powder	50787-0053BULK INGREDIENT
-	PIRFENIDONE	powder	50787-0009BULK INGREDIENT

Compare

Comparable companies in Mexico

Sicor de Mexico S.A. de C.V.1 site · 27 NDC
Avon Cosmetics Manufacturing, S. de R.L. de C.V.1 site · 16 NDC
Holiday Labs Mexico, S.A. de C.V.1 site · 15 NDC
Interquim, S.A. de C.V.1 site · 14 NDC
Bayer de Mexico, S.A. de C.V.1 site · 10 NDC
Nouryon Chemicals, S.A. de C.V1 site · 8 NDC
Laboratorios Imperiales, S.A. de C.V.1 site · 7 NDC
Laboratorios Zeyco SA de CV1 site · 5 NDC
Fermic, S.A. de C.V.1 site · 4 NDC
Boehringer Ingelheim Promeco S.A. de C.V.1 site · 3 NDC

Enquiry

Common questions

Is Signa S.A. de C.V. FDA approved?: Signa S.A. de C.V. holds 1 FDA-registered establishment in Mexico. Registration puts a site on the FDA's register and open to inspection; it is not an approval of the company. Approvals attach to individual drug applications.
Where are Signa S.A. de C.V.'s drugs manufactured?: The FDA register lists Toluca. Registered operations: analytical testing, active ingredient (API) manufacture.
What drugs does Signa S.A. de C.V. make?: 9 products are listed under Signa S.A. de C.V. in the openFDA NDC Directory, most often as powder. The full breakdown by dosage form and route is above. A listing count is not a sales figure.

Compiled from FDA establishment registrations, the openFDA NDC Directory, the Orange Book and the FDA drug shortage database. Not claimed by the company. Sources and methodology.