Chongqing DaXin Pharmaceutical
NDC Database

Chongqing DaXin 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 9
  • Latest Marketing Date 2026-06-01
  • Data Source FDA
  • First Marketing Date 2010-07-28
Company Overview

Company

Chongqing DaXin Pharmaceutical

Country

China

Website

Visit Website

Email

suyh@daxinpharm.com

Social Profiles

Company Snapshot

Chongqing DaXin Pharmaceutical

China Chongqing Beibei create Road No. 22

China

www.daxinpharm.com/ suyh@daxinpharm.com View on Map
NDC Records ( 9 records )
2010
28 Jul
Bulk Ingredient NDC: 57885-0002

Nonproprietary Name

Tobramycin

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Chongqing Daxin Pharmaceutical Co. Ltd.

Marketing Category

BULK INGREDIENT

57885-0002

Substance

TOBRAMYCIN

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2010-07-28

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2020
01 Jan
Bulk Ingredient NDC: 57885-0009

Nonproprietary Name

Mycophenolic Acid

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Chongqing Daxin Pharmaceutical Co. Ltd.

Marketing Category

BULK INGREDIENT

57885-0009

Substance

MYCOPHENOLIC ACID

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2020-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2013
08 Oct
Bulk Ingredient NDC: 57885-0010

Nonproprietary Name

moxidectin

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Chongqing Daxin Pharmaceutical Co. Ltd.

Marketing Category

BULK INGREDIENT

57885-0010

Substance

MOXIDECTIN

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2013-10-08

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2020
01 Jan
Bulk Ingredient NDC: 57885-0011

Nonproprietary Name

Daptomycin

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Chongqing Daxin Pharmaceutical Co. Ltd.

Marketing Category

BULK INGREDIENT

57885-0011

Substance

DAPTOMYCIN

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2020-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2020
01 Jan
Bulk Ingredient NDC: 57885-0012

Nonproprietary Name

Vancomycin HCl

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Chongqing Daxin Pharmaceutical Co. Ltd.

Marketing Category

BULK INGREDIENT

57885-0012

Substance

VANCOMYCIN HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2020-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2020
01 Jan
Bulk Ingredient NDC: 57885-0014

Nonproprietary Name

Sirolimus

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Chongqing Daxin Pharmaceutical Co. Ltd.

Marketing Category

BULK INGREDIENT

57885-0014

Substance

SIROLIMUS

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2020-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2026
01 Jun
Bulk Ingredient NDC: 57885-0014

Nonproprietary Name

Sirolimus

Dosage Form

POWDER

Strength

1 g/g

Labeler

Chongqing Daxin Pharmaceutical Co. Ltd.

Marketing Category

BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING

57885-0014

Substance

SIROLIMUS

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2026-06-01

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2020
01 Jan
Bulk Ingredient NDC: 57885-0015

Nonproprietary Name

Mevastatin

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Chongqing Daxin Pharmaceutical Co. Ltd.

Marketing Category

BULK INGREDIENT

57885-0015

Substance

MEVASTATIN

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2020-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2020
01 Jan
Bulk Ingredient NDC: 57885-0016

Nonproprietary Name

Milbemycin Oxime

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Chongqing Daxin Pharmaceutical Co. Ltd.

Marketing Category

BULK INGREDIENT

57885-0016

Substance

MILBEMYCIN OXIME

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2020-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

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NDC Type Breakdown
9 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).

Visit FDA NDC Directory
NDC Record Details Preview

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

NDC

57885-0002

Nonproprietary Name

Tobramycin

Labeler

Chongqing Daxin Pharmaceutical Co. Ltd.

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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