Qilu Antibiotics Pharmaceutical Co., Ltd.
NDC Database

Qilu Antibiotics 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 2022-06-28
  • Data Source FDA
  • First Marketing Date 1998-10-01
Company Overview

Company

Qilu Antibiotics Pharmaceutical Co., Ltd.

Country

China

Website

Visit Website

Email

hanwei.chen@qilu-antibiotics.com

Social Profiles

Company Snapshot

Qilu Antibiotics Pharmaceutical Co., Ltd.

NO.849, Dongjia Town, Licheng District, Jinan City 250105

China

e.qilu-antibiotics.com hanwei.chen@qilu-antibiotics.com View on Map
NDC Records ( 6 records )
2008
01 Jan
Bulk Ingredient NDC: 51810-001

Nonproprietary Name

sterile cefazolin sodium

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Qilu Antibiotics Pharmaceutical Co., Ltd.

Marketing Category

BULK INGREDIENT

51810-001

Substance

CEFAZOLIN SODIUM

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2008-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

1998
01 Oct
Bulk Ingredient NDC: 51810-002

Nonproprietary Name

sterile ceftriaxone sodium

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Qilu Antibiotics Pharmaceutical Co., Ltd.

Marketing Category

BULK INGREDIENT

51810-002

Substance

CEFTRIAXONE SODIUM

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

1998-10-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2020
04 Apr
Bulk Ingredient NDC: 51810-006

Nonproprietary Name

sterile ceftazidime with sodium carbonate

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Qilu Antibiotics Pharmaceutical Co., Ltd.

Marketing Category

BULK INGREDIENT

51810-006

Substance

CEFTAZIDIME

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2020-04-04

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2011
01 Jan
Bulk Ingredient NDC: 51810-007

Nonproprietary Name

sterile cefepime dihydrochloride with arginine

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Qilu Antibiotics Pharmaceutical Co., Ltd.

Marketing Category

BULK INGREDIENT

51810-007

Substance

CEFEPIME HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2011-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2011
01 Jan
Bulk Ingredient NDC: 51810-009

Nonproprietary Name

sterile cefepime hydrochloride

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Qilu Antibiotics Pharmaceutical Co., Ltd.

Marketing Category

BULK INGREDIENT

51810-009

Substance

CEFEPIME HYDROCHLORIDE

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2011-01-01

End Marketing Date

-

Listing Record Certified Through

2026-12-31

2022
28 Jun
Bulk Ingredient NDC: 51810-052

Nonproprietary Name

cefpodoxime proxetil

Dosage Form

POWDER

Strength

1 kg/kg

Labeler

Qilu Antibiotics Pharmaceutical Co., Ltd.

Marketing Category

BULK INGREDIENT

51810-052

Substance

CEFPODOXIME PROXETIL

Product Type

BULK INGREDIENT

DEA Schedule

Start Marketing Date

2022-06-28

End Marketing Date

-

Listing Record Certified Through

2026-12-31

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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

51810-001

Nonproprietary Name

sterile cefazolin sodium

Labeler

Qilu Antibiotics Pharmaceutical Co., Ltd.

Dosage Form

POWDER

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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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