Qilu Antibiotics Pharmaceutical Co., Ltd.
FDA Approved Drugs

Qilu Antibiotics Pharmaceutical Co., Ltd.

FDA Approved Drugs Database

FDA approved drug product records including application numbers, product numbers, drug names, active ingredients, dosage forms, strengths, approval dates and regulatory status.

RX
  • Total Records 13
  • Latest Approval Date Oct 31, 2024
  • Data Source FDA
  • First Approval Date Dec 28, 2015
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
FDA Approved Drug Records ( 13 records )
2015
28 Dec
RX Application: 203661

Drug Name

CEFAZOLIN SODIUM

Product Number

1

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

2015-12-28

203661 / 1

Active Ingredient

CEFAZOLIN SODIUM

Application Number

203661

Product Number

1

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

2015-12-28

Regulatory Status

RX

2022
11 Mar
RX Application: 203661

Drug Name

CEFAZOLIN SODIUM

Product Number

2

Dosage Form

-

Strength

EQ 2GM BASE/VIAL

Approval Date

2022-03-11

203661 / 2

Active Ingredient

CEFAZOLIN SODIUM

Application Number

203661

Product Number

2

Dosage Form

-

Strength

EQ 2GM BASE/VIAL

Approval Date

2022-03-11

Regulatory Status

RX

2024
24 Jan
RX Application: 203661

Drug Name

CEFAZOLIN SODIUM

Product Number

3

Dosage Form

-

Strength

EQ 3GM BASE/VIAL

Approval Date

2024-01-24

203661 / 3

Active Ingredient

CEFAZOLIN SODIUM

Application Number

203661

Product Number

3

Dosage Form

-

Strength

EQ 3GM BASE/VIAL

Approval Date

2024-01-24

Regulatory Status

RX

2018
17 Oct
RX Application: 209217

Drug Name

CEFAZOLIN SODIUM

Product Number

1

Dosage Form

-

Strength

EQ 10GM BASE/VIAL

Approval Date

2018-10-17

209217 / 1

Active Ingredient

CEFAZOLIN SODIUM

Application Number

209217

Product Number

1

Dosage Form

-

Strength

EQ 10GM BASE/VIAL

Approval Date

2018-10-17

Regulatory Status

RX

2016
01 Feb
RX Application: 203704

Drug Name

CEFEPIME HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE/VIAL

Approval Date

2016-02-01

203704 / 1

Active Ingredient

CEFEPIME HYDROCHLORIDE

Application Number

203704

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE/VIAL

Approval Date

2016-02-01

Regulatory Status

RX

2016
01 Feb
RX Application: 203704

Drug Name

CEFEPIME HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

2016-02-01

203704 / 2

Active Ingredient

CEFEPIME HYDROCHLORIDE

Application Number

203704

Product Number

2

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

2016-02-01

Regulatory Status

RX

2016
01 Feb
RX Application: 203704

Drug Name

CEFEPIME HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

EQ 2GM BASE/VIAL

Approval Date

2016-02-01

203704 / 3

Active Ingredient

CEFEPIME HYDROCHLORIDE

Application Number

203704

Product Number

3

Dosage Form

-

Strength

EQ 2GM BASE/VIAL

Approval Date

2016-02-01

Regulatory Status

RX

2016
29 Jun
RX Application: 203702

Drug Name

CEFTRIAXONE

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE/VIAL

Approval Date

2016-06-29

203702 / 1

Active Ingredient

CEFTRIAXONE SODIUM

Application Number

203702

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE/VIAL

Approval Date

2016-06-29

Regulatory Status

RX

2016
29 Jun
RX Application: 203702

Drug Name

CEFTRIAXONE

Product Number

2

Dosage Form

-

Strength

EQ 500MG BASE/VIAL

Approval Date

2016-06-29

203702 / 2

Active Ingredient

CEFTRIAXONE SODIUM

Application Number

203702

Product Number

2

Dosage Form

-

Strength

EQ 500MG BASE/VIAL

Approval Date

2016-06-29

Regulatory Status

RX

2016
29 Jun
RX Application: 203702

Drug Name

CEFTRIAXONE

Product Number

3

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

2016-06-29

203702 / 3

Active Ingredient

CEFTRIAXONE SODIUM

Application Number

203702

Product Number

3

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

2016-06-29

Regulatory Status

RX

2016
29 Jun
RX Application: 203702

Drug Name

CEFTRIAXONE

Product Number

4

Dosage Form

-

Strength

EQ 2GM BASE/VIAL

Approval Date

2016-06-29

203702 / 4

Active Ingredient

CEFTRIAXONE SODIUM

Application Number

203702

Product Number

4

Dosage Form

-

Strength

EQ 2GM BASE/VIAL

Approval Date

2016-06-29

Regulatory Status

RX

2018
17 Oct
RX Application: 209218

Drug Name

CEFTRIAXONE

Product Number

1

Dosage Form

-

Strength

EQ 10GM BASE/VIAL

Approval Date

2018-10-17

209218 / 1

Active Ingredient

CEFTRIAXONE SODIUM

Application Number

209218

Product Number

1

Dosage Form

-

Strength

EQ 10GM BASE/VIAL

Approval Date

2018-10-17

Regulatory Status

RX

2024
31 Oct
RX Application: 218067

Drug Name

ERTAPENEM SODIUM

Product Number

1

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

2024-10-31

218067 / 1

Active Ingredient

ERTAPENEM SODIUM

Application Number

218067

Product Number

1

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

Approval Date

2024-10-31

Regulatory Status

RX

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Drug Status Breakdown
13 total
  • RX
Official Source

FDA approved drug data is based on publicly available U.S. Food and Drug Administration Orange Book information.

Visit FDA Orange Book
FDA Approved Drug Record Details Preview

Explore important FDA approved drug information available in the records above.

Drug Name

CEFAZOLIN SODIUM

Application Number

203661

Product Number

1

Active Ingredient

CEFAZOLIN SODIUM

Dosage Form

-

Strength

EQ 1GM BASE/VIAL

FDA Approved Drug Data

Approved drug product information

Regular Updates

Data maintained from official sources

Structured Database

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