Laboratorios Imperiales, S.A. de C.V.
NDC Database

Laboratorios Imperiales, 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 7
  • Latest Marketing Date 2015-04-16
  • Data Source FDA
  • First Marketing Date 1986-01-02
Company Overview

Company

Laboratorios Imperiales, S.A. de C.V.

Country

Mexico

Website

Email

info@limsa.co

Social Profiles

Company Snapshot

Laboratorios Imperiales, S.A. de C.V.

Calle 13-E No. 606 CIVAC Juitepec, Morelos C.P. 62500 Cuernavaca

Mexico

info@limsa.co View on Map
NDC Records ( 7 records )
2014
13 Nov
Bulk Ingredient NDC: 57465-150

Nonproprietary Name

BISMUTH SUBCARBONATE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Laboratorios Imperiales, S.A. de C.V.

Marketing Category

BULK INGREDIENT

57465-150

Substance

BISMUTH SUBCARBONATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2014-11-13

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2012
22 May
Bulk Ingredient NDC: 57465-151

Nonproprietary Name

BISMUTH SUBNITRATE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Laboratorios Imperiales, S.A. de C.V.

Marketing Category

BULK INGREDIENT

57465-151

Substance

BISMUTH SUBNITRATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2012-05-22

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2015
16 Apr
Bulk Ingredient NDC: 57465-152

Nonproprietary Name

Bismuth Tribromophenate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Laboratorios Imperiales, S.A. de C.V.

Marketing Category

BULK INGREDIENT

57465-152

Substance

BISMUTH TRIBROMOPHENATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2015-04-16

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1986
02 Jan
Bulk Ingredient NDC: 57465-200

Nonproprietary Name

Bismuth Subsalicylate

Dosage Form

POWDER

Strength

50 kg/50kg

Labeler

Laboratorios Imperiales, S.A. de C.V.

Marketing Category

BULK INGREDIENT

57465-200

Substance

BISMUTH SUBSALICYLATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

1986-01-02

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2012
22 May
Bulk Ingredient NDC: 57465-201

Nonproprietary Name

BISMUTH SUBGALLATE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Laboratorios Imperiales, S.A. de C.V.

Marketing Category

BULK INGREDIENT

57465-201

Substance

BISMUTH SUBGALLATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2012-05-22

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2012
22 May
Bulk Ingredient NDC: 57465-202

Nonproprietary Name

BISMUTH CITRATE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Laboratorios Imperiales, S.A. de C.V.

Marketing Category

BULK INGREDIENT

57465-202

Substance

BISMUTH CITRATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2012-05-22

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1986
02 Jan
Bulk Ingredient NDC: 57465-300

Nonproprietary Name

BISMUTH OXIDE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Laboratorios Imperiales, S.A. de C.V.

Marketing Category

BULK INGREDIENT

57465-300

Substance

BISMUTH OXIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

1986-01-02

End Marketing Date

-

Listing Record Certified Through

2026-12-31

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NDC Type Breakdown
7 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).

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NDC Record Details Preview

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

NDC

57465-150

Nonproprietary Name

BISMUTH SUBCARBONATE

Labeler

Laboratorios Imperiales, S.A. de C.V.

Dosage Form

POWDER

FDA NDC Data

National Drug Code information

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Data maintained from official sources

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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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