Inga Pharmaceuticals
NDC Database

Inga Pharmaceuticals

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 4
  • Latest Marketing Date 2023-07-01
  • Data Source FDA
  • First Marketing Date 1999-09-01
Company Overview

Company

Inga Pharmaceuticals

Country

India

Website

Visit Website

Email

info@ingapharma.com

Social Profiles

Company Snapshot

Inga Pharmaceuticals

Inga House, Mahakali Road, Andheri East, Mumbai – 400093

India

www.ingapharma.com/ info@ingapharma.com View on Map
NDC Records ( 4 records )
1999
01 Sep
Bulk Ingredient NDC: 63570-008

Nonproprietary Name

Podophyllum Resin

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Inga Pharmaceuticals

Marketing Category

BULK INGREDIENT

63570-008

Substance

PODOPHYLLUM RESIN

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

1999-09-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2000
01 Mar
Bulk Ingredient NDC: 63570-010

Nonproprietary Name

Belladonna Extract

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Inga Pharmaceuticals

Marketing Category

BULK INGREDIENT

63570-010

Substance

ATROPA BELLADONNA

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2000-03-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2000
01 Mar
Bulk Ingredient NDC: 63570-011

Nonproprietary Name

Belladonna Tincture

Dosage Form

LIQUID

Strength

1 kg/kg

Labeler

Inga Pharmaceuticals

Marketing Category

BULK INGREDIENT

63570-011

Substance

ATROPA BELLADONNA

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2000-03-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2023
01 Jul
Bulk Ingredient NDC: 63570-030

Nonproprietary Name

Papaverine Hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Inga Pharmaceuticals

Marketing Category

BULK INGREDIENT

63570-030

Substance

PAPAVERINE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2023-07-01

End Marketing Date

-

Listing Record Certified Through

2027-12-31

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NDC Type Breakdown
4 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

63570-008

Nonproprietary Name

Podophyllum Resin

Labeler

Inga Pharmaceuticals

Dosage Form

POWDER

FDA NDC Data

National Drug Code information

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Data maintained from official sources

Structured Database

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

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