Huzhou Zhanwang Pharmaceutical Co.,Ltd.
NDC Database

Huzhou Zhanwang 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 7
  • Latest Marketing Date 2017-12-18
  • Data Source FDA
  • First Marketing Date 2011-02-22
Company Overview

Company

Huzhou Zhanwang Pharmaceutical Co.,Ltd.

Country

China

Website

Visit Website

Email

sales@zhanwangpharma.com

Social Profiles

Company Snapshot

Huzhou Zhanwang Pharmaceutical Co.,Ltd.

No.1 Jiefang Rd Linghu Town Huzhou City Zhejiang Province, China

China

www.zhanwangpharma.com/ sales@zhanwangpharma.com View on Map
NDC Records ( 7 records )
2017
18 Dec
Bulk Ingredient NDC: 63660-0006

Nonproprietary Name

Methotrexate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Huzhou Zhanwang Pharmaceutical Co. Ltd

Marketing Category

BULK INGREDIENT

63660-0006

Substance

METHOTREXATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2017-12-18

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2011
22 Feb
Bulk Ingredient NDC: 63660-0010

Nonproprietary Name

Azacitidine

Dosage Form

POWDER

Strength

1 g/g

Labeler

Huzhou Zhanwang Pharmaceutical Co. Ltd

Marketing Category

BULK INGREDIENT

63660-0010

Substance

AZACITIDINE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2011-02-22

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2011
01 Mar
Bulk Ingredient NDC: 63660-0002

Nonproprietary Name

Milrinone

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Huzhou Zhanwang Pharmaceutical Co., Ltd.

Marketing Category

BULK INGREDIENT

63660-0002

Substance

MILRINONE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2011-03-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2011
01 Mar
Bulk Ingredient NDC: 63660-0004

Nonproprietary Name

Esmolol Hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Huzhou Zhanwang Pharmaceutical Co., Ltd.

Marketing Category

BULK INGREDIENT

63660-0004

Substance

ESMOLOL HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2011-03-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2011
01 Mar
Bulk Ingredient NDC: 63660-0005

Nonproprietary Name

Etomidate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Huzhou Zhanwang Pharmaceutical Co., Ltd.

Marketing Category

BULK INGREDIENT

63660-0005

Substance

ETOMIDATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2011-03-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2011
24 Feb
Bulk Ingredient NDC: 63660-0008

Nonproprietary Name

Pemetrexed Disodium

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Huzhou Zhanwang Pharmaceutical Co., Ltd.

Marketing Category

BULK INGREDIENT

63660-0008

Substance

PEMETREXED DISODIUM

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2011-02-24

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2012
25 Oct
Bulk Ingredient NDC: 63660-0012

Nonproprietary Name

LEUCOVORIN CALCIUM

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Huzhou Zhanwang Pharmaceutical Co., Ltd.

Marketing Category

BULK INGREDIENT

63660-0012

Substance

LEUCOVORIN CALCIUM

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2012-10-25

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

63660-0006

Nonproprietary Name

Methotrexate

Labeler

Huzhou Zhanwang Pharmaceutical Co. Ltd

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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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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