FUJIAN FUKANG PHARMACEUTICAL CO., LTD.
NDC Database

FUJIAN FUKANG 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 6
  • Latest Marketing Date 2026-02-13
  • Data Source FDA
  • First Marketing Date 2011-02-16
Company Overview

Company

FUJIAN FUKANG PHARMACEUTICAL CO., LTD.

Country

China

Website

Visit Website

Email

fukang@fz-antibiotic.com

Social Profiles

Company Snapshot

FUJIAN FUKANG PHARMACEUTICAL CO., LTD.

NO.138, Xiangban Road, Fuzhou 350002

China

www.fz-antibiotic.com/ fukang@fz-antibiotic.com View on Map
NDC Records ( 6 records )
2011
09 Mar
Bulk Ingredient NDC: 67630-0003

Nonproprietary Name

GENTAMICIN SULFATE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

FUJIAN FUKANG PHARMACEUTICAL CO., LTD

Marketing Category

BULK INGREDIENT

67630-0003

Substance

GENTAMICIN SULFATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2011-03-09

End Marketing Date

-

Listing Record Certified Through

2027-12-31

2011
16 Feb
Bulk Ingredient NDC: 67630-0008

Nonproprietary Name

CHLORTETRACYCLINE HYDROCHLORIDE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

FUJIAN FUKANG PHARMACEUTICAL CO., LTD

Marketing Category

BULK INGREDIENT

67630-0008

Substance

CHLORTETRACYCLINE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2011-02-16

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2018
07 Sep
Bulk Ingredient NDC: 67630-0007

Nonproprietary Name

TETRACYCLINE HYDROCHLORIDE

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

FUJIAN FUKANG PHARMACEUTICAL CO., LTD.

Marketing Category

BULK INGREDIENT

67630-0007

Substance

TETRACYCLINE HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2018-09-07

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2025
31 Jul
Bulk Ingredient NDC: 67630-0010

Nonproprietary Name

Oseltamivir Epoxide

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

FUJIAN FUKANG PHARMACEUTICAL CO., LTD.

Marketing Category

BULK INGREDIENT

67630-0010

Substance

ETHYL (1S,5R,6S)-5-(1-ETHYLPROPOXY)-7-OXABICYCLO(4.1.0)HEPT-3-ENE-3-CARBOXYLATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2025-07-31

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2025
31 Jul
Bulk Ingredient NDC: 67630-0013

Nonproprietary Name

Oseltamivir Phosphate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

FUJIAN FUKANG PHARMACEUTICAL CO., LTD.

Marketing Category

BULK INGREDIENT

67630-0013

Substance

OSELTAMIVIR PHOSPHATE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2025-07-31

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2026
13 Feb
Bulk Ingredient NDC: 67630-0016

Nonproprietary Name

Nystatin

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

FUJIAN FUKANG PHARMACEUTICAL CO., LTD.

Marketing Category

BULK INGREDIENT

67630-0016

Substance

NYSTATIN

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2026-02-13

End Marketing Date

-

Listing Record Certified Through

2027-12-31

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NDC Type Breakdown
6 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

67630-0003

Nonproprietary Name

GENTAMICIN SULFATE

Labeler

FUJIAN FUKANG 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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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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