Chongqing Huapont Pharmaceutical
NDC Database

Chongqing Huapont Pharmaceutical

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 2022-01-14
  • Data Source FDA
  • First Marketing Date 2000-01-01
Company Overview

Company

Chongqing Huapont Pharmaceutical

Country

China

Website

Visit Website

Email

api@huapont.cn

Social Profiles

Company Snapshot

Chongqing Huapont Pharmaceutical

No.69 Xingguang Avenue, Renhe Town, Yubei District, Chongqing

China

www.huapont.cn/index.html api@huapont.cn View on Map
NDC Records ( 7 records )
2003
01 Jan
Bulk Ingredient NDC: 48943-0010

Nonproprietary Name

Isotretinoin

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Chongqing Huapont Pharmaceutical Co Limited

Marketing Category

BULK INGREDIENT

48943-0010

Substance

ISOTRETINOIN

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2003-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2011
10 Mar
Bulk Ingredient NDC: 48943-0012

Nonproprietary Name

Alitretinoin

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Chongqing Huapont Pharmaceutical Co Limited

Marketing Category

BULK INGREDIENT

48943-0012

Substance

ALITRETINOIN

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2011-03-10

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2011
10 Mar
Bulk Ingredient NDC: 48943-0013

Nonproprietary Name

Bexarotene

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Chongqing Huapont Pharmaceutical Co Limited

Marketing Category

BULK INGREDIENT

48943-0013

Substance

BEXAROTENE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2011-03-10

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2011
31 Mar
Bulk Ingredient NDC: 48943-0014

Nonproprietary Name

Micronized Bexarotene

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Chongqing Huapont Pharmaceutical Co Limited

Marketing Category

BULK INGREDIENT

48943-0014

Substance

BEXAROTENE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2011-03-31

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2011
10 Mar
Bulk Ingredient NDC: 48943-0015

Nonproprietary Name

Tetrandrine

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Chongqing Huapont Pharmaceutical Co Limited

Marketing Category

BULK INGREDIENT

48943-0015

Substance

TETRANDRINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2011-03-10

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2000
01 Jan
Bulk Ingredient NDC: 48943-0011

Nonproprietary Name

Tretinoin

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Chongqing Huapont Pharmaceutical Co Ltd

Marketing Category

BULK INGREDIENT

48943-0011

Substance

TRETINOIN

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2000-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2022
14 Jan
Bulk Ingredient NDC: 48943-0033

Nonproprietary Name

Paricalcitol

Dosage Form

POWDER

Strength

1 g/g

Labeler

Chongqing Huapont Pharmaceutical Co Ltd

Marketing Category

BULK INGREDIENT

48943-0033

Substance

PARICALCITOL

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2022-01-14

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

48943-0010

Nonproprietary Name

Isotretinoin

Labeler

Chongqing Huapont Pharmaceutical Co Limited

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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