Signa S.A. de C.V.
NDC Database

Signa S.A. de C.V.

NDC Database

National Drug Code (NDC) records including drug products, NDC numbers, nonproprietary names, dosage forms, strengths, labelers and marketing information.

Bulk Ingredient
  • Total Records 9
  • Latest Marketing Date 2014-12-22
  • Data Source FDA
  • First Marketing Date 2000-11-30
Company Overview

Company

Signa S.A. de C.V.

Country

Mexico

Website

Email

Social Profiles

Company Snapshot

Signa S.A. de C.V.

Industria Automotriz No 301, Toluca, Estado De Mexico

Mexico

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NDC Records ( 9 records )
2000
30 Nov
Bulk Ingredient NDC: 50787-0009

Nonproprietary Name

PIRFENIDONE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Signa S.A. de C.V.

Marketing Category

BULK INGREDIENT

50787-0009

Substance

PIRFENIDONE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2000-11-30

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2009
09 Apr
Bulk Ingredient NDC: 50787-0016

Nonproprietary Name

FAMCICLOVIR

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Signa S.A. de C.V.

Marketing Category

BULK INGREDIENT

50787-0016

Substance

FAMCICLOVIR

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2009-04-09

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2001
13 Nov
Bulk Ingredient NDC: 50787-0022

Nonproprietary Name

CLOPIDOGREL

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Signa S.A. de C.V.

Marketing Category

BULK INGREDIENT

50787-0022

Substance

CLOPIDOGREL BISULFATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2001-11-13

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2009
08 Jul
Bulk Ingredient NDC: 50787-0027

Nonproprietary Name

LAMIVUDINE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Signa S.A. de C.V.

Marketing Category

BULK INGREDIENT

50787-0027

Substance

LAMIVUDINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2009-07-08

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2005
21 Oct
Bulk Ingredient NDC: 50787-0032

Nonproprietary Name

BALSALAZIDE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Signa S.A. de C.V.

Marketing Category

BULK INGREDIENT

50787-0032

Substance

BALSALAZIDE DISODIUM

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2005-10-21

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2009
16 Jul
Bulk Ingredient NDC: 50787-0037

Nonproprietary Name

ACYCLOVIR

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Signa S.A. de C.V.

Marketing Category

BULK INGREDIENT

50787-0037

Substance

ACYCLOVIR

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2009-07-16

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2008
30 Jul
Bulk Ingredient NDC: 50787-0040

Nonproprietary Name

DULOXETINE HYDROCHLORIDE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Signa S.A. de C.V.

Marketing Category

BULK INGREDIENT

50787-0040

Substance

DULOXETINE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2008-07-30

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2014
22 Dec
Bulk Ingredient NDC: 50787-0053

Nonproprietary Name

PAROXETINE HYDROCHLORIDE HEMIHYDRATE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Signa S.A. de C.V.

Marketing Category

BULK INGREDIENT

50787-0053

Substance

PAROXETINE HYDROCHLORIDE HEMIHYDRATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2014-12-22

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2008
29 Apr
Bulk Ingredient NDC: 50787-0059

Nonproprietary Name

ATORVASTATIN CALCIUM PROPYLENE GLYCOL SOLVATE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Signa S.A. de C.V.

Marketing Category

BULK INGREDIENT

50787-0059

Substance

ATORVASTATIN CALCIUM PROPYLENE GLYCOL SOLVATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2008-04-29

End Marketing Date

-

Listing Record Certified Through

2026-12-31

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NDC Type Breakdown
9 total
  • Bulk Ingredient
Official Source

NDC data is based on publicly available National Drug Code information from the U.S. Food and Drug Administration (FDA).

Visit FDA NDC Directory
NDC Record Details Preview

Explore important National Drug Code information available in the records above.

NDC

50787-0009

Nonproprietary Name

PIRFENIDONE

Labeler

Signa S.A. de C.V.

Dosage Form

POWDER

FDA NDC Data

National Drug Code information

Regular Updates

Data maintained from official sources

Structured Database

Searchable pharmaceutical data

Reliable Data

Organized NDC records

NDC data is based on publicly available U.S. Food and Drug Administration (FDA) National Drug Code information.

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