Cheplapharm Arzneimittel Gmbh Discontinued
FDA Approved Drugs

Cheplapharm Arzneimittel Gmbh Discontinued

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.

Discontinued
  • Total Records 7
  • Latest Approval Date Dec 20, 1998
  • Data Source FDA
  • First Approval Date Jun 23, 1989
All
31
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Unclassified
4
View
Discontinued
7
View
RX
20
View
Company Overview

Company

Cheplapharm Arzneimittel Gmbh Discontinued

Country

Germany

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Company Snapshot

Cheplapharm Arzneimittel Gmbh Discontinued

BAHNHOFSTR. 1A

Germany

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FDA Approved Drug Records ( 7 records )
1989
23 Jun
Discontinued Application: 19661

Drug Name

CYTOVENE

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1989-06-23

19661 / 1

Active Ingredient

GANCICLOVIR SODIUM

Application Number

19661

Product Number

1

Dosage Form

-

Strength

EQ 500MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1989-06-23

Regulatory Status

Discontinued

1997
09 Apr
Discontinued Application: 17533

Drug Name

KLONOPIN

Product Number

5

Dosage Form

-

Strength

0.125MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1997-04-09

17533 / 5

Active Ingredient

CLONAZEPAM

Application Number

17533

Product Number

5

Dosage Form

-

Strength

0.125MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1997-04-09

Regulatory Status

Discontinued

1997
09 Apr
Discontinued Application: 17533

Drug Name

KLONOPIN

Product Number

6

Dosage Form

-

Strength

0.25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1997-04-09

17533 / 6

Active Ingredient

CLONAZEPAM

Application Number

17533

Product Number

6

Dosage Form

-

Strength

0.25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1997-04-09

Regulatory Status

Discontinued

1998
20 Dec
Discontinued Application: 20639

Drug Name

SEROQUEL

Product Number

4

Dosage Form

-

Strength

EQ 150MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1998-12-20

20639 / 4

Active Ingredient

QUETIAPINE FUMARATE

Application Number

20639

Product Number

4

Dosage Form

-

Strength

EQ 150MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1998-12-20

Regulatory Status

Discontinued

1995
22 Nov
Discontinued Application: 20438

Drug Name

VESANOID

Product Number

1

Dosage Form

-

Strength

10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1995-11-22

20438 / 1

Active Ingredient

TRETINOIN

Application Number

20438

Product Number

1

Dosage Form

-

Strength

10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1995-11-22

Regulatory Status

Discontinued

1998
30 Apr
Discontinued Application: 20896

Drug Name

XELODA

Product Number

1

Dosage Form

-

Strength

150MG

Approval Date

1998-04-30

20896 / 1

Active Ingredient

CAPECITABINE

Application Number

20896

Product Number

1

Dosage Form

-

Strength

150MG

Approval Date

1998-04-30

Regulatory Status

Discontinued

1998
30 Apr
Discontinued Application: 20896

Drug Name

XELODA

Product Number

2

Dosage Form

-

Strength

500MG

Approval Date

1998-04-30

20896 / 2

Active Ingredient

CAPECITABINE

Application Number

20896

Product Number

2

Dosage Form

-

Strength

500MG

Approval Date

1998-04-30

Regulatory Status

Discontinued

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Drug Status Breakdown
7 total
  • Discontinued
Official Source

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

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

Drug Name

CYTOVENE

Application Number

19661

Product Number

1

Active Ingredient

GANCICLOVIR SODIUM

Dosage Form

-

Strength

EQ 500MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

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