Yung Shin Pharmaceutical Industrial RX
FDA Approved Drugs

Yung Shin Pharmaceutical Industrial RX

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 20
  • Latest Approval Date Nov 10, 2021
  • Data Source FDA
  • First Approval Date Jan 22, 2004
All
25
View
Discontinued
5
View
RX
20
View
Company Overview

Company

Yung Shin Pharmaceutical Industrial RX

Country

China

Website

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Company Snapshot

Yung Shin Pharmaceutical Industrial RX

Lujia Town, KunShan City, JiangSu Province

China

www.yungshingroup.com/en/category/view.aspx?r=58 View on Map
FDA Approved Drug Records ( 20 records )
2004
22 Jan
RX Application: 65146

Drug Name

CEFACLOR

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

2004-01-22

65146 / 1

Active Ingredient

CEFACLOR

Application Number

65146

Product Number

1

Dosage Form

-

Strength

EQ 250MG BASE

Approval Date

2004-01-22

Regulatory Status

RX

2004
22 Jan
RX Application: 65146

Drug Name

CEFACLOR

Product Number

2

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

2004-01-22

65146 / 2

Active Ingredient

CEFACLOR

Application Number

65146

Product Number

2

Dosage Form

-

Strength

EQ 500MG BASE

Approval Date

2004-01-22

Regulatory Status

RX

2012
17 Feb
RX Application: 65412

Drug Name

CEFACLOR

Product Number

1

Dosage Form

-

Strength

EQ 125MG BASE/5ML

Approval Date

2012-02-17

65412 / 1

Active Ingredient

CEFACLOR

Application Number

65412

Product Number

1

Dosage Form

-

Strength

EQ 125MG BASE/5ML

Approval Date

2012-02-17

Regulatory Status

RX

2012
17 Feb
RX Application: 65412

Drug Name

CEFACLOR

Product Number

2

Dosage Form

-

Strength

EQ 187MG BASE/5ML

Approval Date

2012-02-17

65412 / 2

Active Ingredient

CEFACLOR

Application Number

65412

Product Number

2

Dosage Form

-

Strength

EQ 187MG BASE/5ML

Approval Date

2012-02-17

Regulatory Status

RX

2012
17 Feb
RX Application: 65412

Drug Name

CEFACLOR

Product Number

3

Dosage Form

-

Strength

EQ 250MG BASE/5ML

Approval Date

2012-02-17

65412 / 3

Active Ingredient

CEFACLOR

Application Number

65412

Product Number

3

Dosage Form

-

Strength

EQ 250MG BASE/5ML

Approval Date

2012-02-17

Regulatory Status

RX

2012
17 Feb
RX Application: 65412

Drug Name

CEFACLOR

Product Number

4

Dosage Form

-

Strength

EQ 375MG BASE/5ML

Approval Date

2012-02-17

65412 / 4

Active Ingredient

CEFACLOR

Application Number

65412

Product Number

4

Dosage Form

-

Strength

EQ 375MG BASE/5ML

Approval Date

2012-02-17

Regulatory Status

RX

2007
25 Jul
RX Application: 65336

Drug Name

CEPHALEXIN

Product Number

1

Dosage Form

-

Strength

EQ 125MG BASE/5ML

Approval Date

2007-07-25

65336 / 1

Active Ingredient

CEPHALEXIN

Application Number

65336

Product Number

1

Dosage Form

-

Strength

EQ 125MG BASE/5ML

Approval Date

2007-07-25

Regulatory Status

RX

2007
25 Jul
RX Application: 65336

Drug Name

CEPHALEXIN

Product Number

2

Dosage Form

-

Strength

EQ 250MG BASE/5ML

Approval Date

2007-07-25

65336 / 2

Active Ingredient

CEPHALEXIN

Application Number

65336

Product Number

2

Dosage Form

-

Strength

EQ 250MG BASE/5ML

Approval Date

2007-07-25

Regulatory Status

RX

2013
13 Jun
RX Application: 202297

Drug Name

CLONIDINE HYDROCHLORIDE

Product Number

1

Dosage Form

-

Strength

0.1MG

Approval Date

2013-06-13

202297 / 1

Active Ingredient

CLONIDINE HYDROCHLORIDE

Application Number

202297

Product Number

1

Dosage Form

-

Strength

0.1MG

Approval Date

2013-06-13

Regulatory Status

RX

2013
13 Jun
RX Application: 202297

Drug Name

CLONIDINE HYDROCHLORIDE

Product Number

2

Dosage Form

-

Strength

0.2MG

Approval Date

2013-06-13

202297 / 2

Active Ingredient

CLONIDINE HYDROCHLORIDE

Application Number

202297

Product Number

2

Dosage Form

-

Strength

0.2MG

Approval Date

2013-06-13

Regulatory Status

RX

2013
13 Jun
RX Application: 202297

Drug Name

CLONIDINE HYDROCHLORIDE

Product Number

3

Dosage Form

-

Strength

0.3MG

Approval Date

2013-06-13

202297 / 3

Active Ingredient

CLONIDINE HYDROCHLORIDE

Application Number

202297

Product Number

3

Dosage Form

-

Strength

0.3MG

Approval Date

2013-06-13

Regulatory Status

RX

2020
19 Feb
RX Application: 205143

Drug Name

DICLOFENAC SODIUM AND MISOPROSTOL

Product Number

1

Dosage Form

-

Strength

50MG;0.2MG

Approval Date

2020-02-19

205143 / 1

Active Ingredient

DICLOFENAC SODIUM; MISOPROSTOL

Application Number

205143

Product Number

1

Dosage Form

-

Strength

50MG;0.2MG

Approval Date

2020-02-19

Regulatory Status

RX

2020
19 Feb
RX Application: 205143

Drug Name

DICLOFENAC SODIUM AND MISOPROSTOL

Product Number

2

Dosage Form

-

Strength

75MG;0.2MG

Approval Date

2020-02-19

205143 / 2

Active Ingredient

DICLOFENAC SODIUM; MISOPROSTOL

Application Number

205143

Product Number

2

Dosage Form

-

Strength

75MG;0.2MG

Approval Date

2020-02-19

Regulatory Status

RX

2021
10 Nov
RX Application: 208195

Drug Name

ENTECAVIR

Product Number

1

Dosage Form

-

Strength

0.5MG

Approval Date

2021-11-10

208195 / 1

Active Ingredient

ENTECAVIR

Application Number

208195

Product Number

1

Dosage Form

-

Strength

0.5MG

Approval Date

2021-11-10

Regulatory Status

RX

2021
10 Nov
RX Application: 208195

Drug Name

ENTECAVIR

Product Number

2

Dosage Form

-

Strength

1MG

Approval Date

2021-11-10

208195 / 2

Active Ingredient

ENTECAVIR

Application Number

208195

Product Number

2

Dosage Form

-

Strength

1MG

Approval Date

2021-11-10

Regulatory Status

RX

2019
29 Apr
RX Application: 204800

Drug Name

FELODIPINE

Product Number

1

Dosage Form

-

Strength

2.5MG

Approval Date

2019-04-29

204800 / 1

Active Ingredient

FELODIPINE

Application Number

204800

Product Number

1

Dosage Form

-

Strength

2.5MG

Approval Date

2019-04-29

Regulatory Status

RX

2019
29 Apr
RX Application: 204800

Drug Name

FELODIPINE

Product Number

2

Dosage Form

-

Strength

5MG

Approval Date

2019-04-29

204800 / 2

Active Ingredient

FELODIPINE

Application Number

204800

Product Number

2

Dosage Form

-

Strength

5MG

Approval Date

2019-04-29

Regulatory Status

RX

2019
29 Apr
RX Application: 204800

Drug Name

FELODIPINE

Product Number

3

Dosage Form

-

Strength

10MG

Approval Date

2019-04-29

204800 / 3

Active Ingredient

FELODIPINE

Application Number

204800

Product Number

3

Dosage Form

-

Strength

10MG

Approval Date

2019-04-29

Regulatory Status

RX

2006
07 Dec
RX Application: 77918

Drug Name

MELOXICAM

Product Number

1

Dosage Form

-

Strength

7.5MG

Approval Date

2006-12-07

77918 / 1

Active Ingredient

MELOXICAM

Application Number

77918

Product Number

1

Dosage Form

-

Strength

7.5MG

Approval Date

2006-12-07

Regulatory Status

RX

2006
07 Dec
RX Application: 77918

Drug Name

MELOXICAM

Product Number

2

Dosage Form

-

Strength

15MG

Approval Date

2006-12-07

77918 / 2

Active Ingredient

MELOXICAM

Application Number

77918

Product Number

2

Dosage Form

-

Strength

15MG

Approval Date

2006-12-07

Regulatory Status

RX

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Drug Status Breakdown
20 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

CEFACLOR

Application Number

65146

Product Number

1

Active Ingredient

CEFACLOR

Dosage Form

-

Strength

EQ 250MG BASE

FDA Approved Drug Data

Approved drug product information

Regular Updates

Data maintained from official sources

Structured Database

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Reliable Data

Organized FDA drug records

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