Zhejiang Jiangbei Pharmaceutical Co., Ltd.
NDC Database

Zhejiang Jiangbei Pharmaceutical Co., Ltd.

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 2
  • Latest Marketing Date 2024-09-30
  • Data Source FDA
  • First Marketing Date 2017-09-01
Company Overview

Company

Zhejiang Jiangbei Pharmaceutical Co., Ltd.

Country

China

Social Profiles

Company Snapshot

Zhejiang Jiangbei Pharmaceutical Co., Ltd.

Dongdai Zhangan Street, Jiaojiang Taizhou, Zhejiang 318017

China

www.jiangbei.com/ hmc@jiangbei.com View on Map
NDC Records ( 2 records )
2017
01 Sep
Bulk Ingredient NDC: 13403-201

Nonproprietary Name

SIMVASTATIN

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Zhejiang Jiangbei Pharmaceutical Co., Ltd.

Marketing Category

BULK INGREDIENT

13403-201

Substance

SIMVASTATIN

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2017-09-01

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2024
30 Sep
Bulk Ingredient NDC: 13403-215

Nonproprietary Name

Atorvastatin calcium trihydrate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Zhejiang Jiangbei Pharmaceutical Co., Ltd.

Marketing Category

BULK INGREDIENT

13403-215

Substance

ATORVASTATIN CALCIUM TRIHYDRATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2024-09-30

End Marketing Date

-

Listing Record Certified Through

2027-12-31

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NDC Type Breakdown
2 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

13403-201

Nonproprietary Name

SIMVASTATIN

Labeler

Zhejiang Jiangbei Pharmaceutical Co., Ltd.

Dosage Form

POWDER

FDA NDC Data

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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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