CEPHALON INC Discontinued
FDA Approved Drugs

CEPHALON INC 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 23
  • Latest Approval Date Sep 13, 2013
  • Data Source FDA
  • First Approval Date Oct 04, 1993
All
31
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Unclassified
1
View
Discontinued
23
View
RX
7
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Company Overview

Company

CEPHALON INC Discontinued

Country

U.S.A

Website

Visit Website

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Company Snapshot

CEPHALON INC Discontinued

4745 Wiley Post Way Salt Lake City, UT 84116

U.S.A

www.tevapharm.com/ View on Map
FDA Approved Drug Records ( 23 records )
1998
04 Nov
Discontinued Application: 20747

Drug Name

ACTIQ

Product Number

1

Dosage Form

-

Strength

EQ 0.2MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1998-11-04

20747 / 1

Active Ingredient

FENTANYL CITRATE

Application Number

20747

Product Number

1

Dosage Form

-

Strength

EQ 0.2MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1998-11-04

Regulatory Status

Discontinued

1998
04 Nov
Discontinued Application: 20747

Drug Name

ACTIQ

Product Number

2

Dosage Form

-

Strength

EQ 0.4MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1998-11-04

20747 / 2

Active Ingredient

FENTANYL CITRATE

Application Number

20747

Product Number

2

Dosage Form

-

Strength

EQ 0.4MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1998-11-04

Regulatory Status

Discontinued

1998
04 Nov
Discontinued Application: 20747

Drug Name

ACTIQ

Product Number

3

Dosage Form

-

Strength

EQ 0.6MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1998-11-04

20747 / 3

Active Ingredient

FENTANYL CITRATE

Application Number

20747

Product Number

3

Dosage Form

-

Strength

EQ 0.6MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1998-11-04

Regulatory Status

Discontinued

1998
04 Nov
Discontinued Application: 20747

Drug Name

ACTIQ

Product Number

4

Dosage Form

-

Strength

EQ 0.8MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1998-11-04

20747 / 4

Active Ingredient

FENTANYL CITRATE

Application Number

20747

Product Number

4

Dosage Form

-

Strength

EQ 0.8MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1998-11-04

Regulatory Status

Discontinued

1998
04 Nov
Discontinued Application: 20747

Drug Name

ACTIQ

Product Number

5

Dosage Form

-

Strength

EQ 1.2MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1998-11-04

20747 / 5

Active Ingredient

FENTANYL CITRATE

Application Number

20747

Product Number

5

Dosage Form

-

Strength

EQ 1.2MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1998-11-04

Regulatory Status

Discontinued

1998
04 Nov
Discontinued Application: 20747

Drug Name

ACTIQ

Product Number

6

Dosage Form

-

Strength

EQ 1.6MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1998-11-04

20747 / 6

Active Ingredient

FENTANYL CITRATE

Application Number

20747

Product Number

6

Dosage Form

-

Strength

EQ 1.6MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1998-11-04

Regulatory Status

Discontinued

1993
04 Oct
Discontinued Application: 20195

Drug Name

FENTANYL

Product Number

1

Dosage Form

-

Strength

EQ 0.2MG BASE

Approval Date

1993-10-04

20195 / 1

Active Ingredient

FENTANYL CITRATE

Application Number

20195

Product Number

1

Dosage Form

-

Strength

EQ 0.2MG BASE

Approval Date

1993-10-04

Regulatory Status

Discontinued

1993
04 Oct
Discontinued Application: 20195

Drug Name

FENTANYL

Product Number

2

Dosage Form

-

Strength

EQ 0.3MG BASE

Approval Date

1993-10-04

20195 / 2

Active Ingredient

FENTANYL CITRATE

Application Number

20195

Product Number

2

Dosage Form

-

Strength

EQ 0.3MG BASE

Approval Date

1993-10-04

Regulatory Status

Discontinued

1993
04 Oct
Discontinued Application: 20195

Drug Name

FENTANYL

Product Number

3

Dosage Form

-

Strength

EQ 0.4MG BASE

Approval Date

1993-10-04

20195 / 3

Active Ingredient

FENTANYL CITRATE

Application Number

20195

Product Number

3

Dosage Form

-

Strength

EQ 0.4MG BASE

Approval Date

1993-10-04

Regulatory Status

Discontinued

1995
30 Oct
Discontinued Application: 20195

Drug Name

FENTANYL

Product Number

7

Dosage Form

-

Strength

EQ 0.1MG BASE

Approval Date

1995-10-30

20195 / 7

Active Ingredient

FENTANYL CITRATE

Application Number

20195

Product Number

7

Dosage Form

-

Strength

EQ 0.1MG BASE

Approval Date

1995-10-30

Regulatory Status

Discontinued

2006
25 Sep
Discontinued Application: 21947

Drug Name

FENTORA

Product Number

1

Dosage Form

-

Strength

EQ 0.1MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2006-09-25

21947 / 1

Active Ingredient

FENTANYL CITRATE

Application Number

21947

Product Number

1

Dosage Form

-

Strength

EQ 0.1MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2006-09-25

Regulatory Status

Discontinued

2006
25 Sep
Discontinued Application: 21947

Drug Name

FENTORA

Product Number

2

Dosage Form

-

Strength

EQ 0.2MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2006-09-25

21947 / 2

Active Ingredient

FENTANYL CITRATE

Application Number

21947

Product Number

2

Dosage Form

-

Strength

EQ 0.2MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2006-09-25

Regulatory Status

Discontinued

2006
25 Sep
Discontinued Application: 21947

Drug Name

FENTORA

Product Number

3

Dosage Form

-

Strength

EQ 0.4MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2006-09-25

21947 / 3

Active Ingredient

FENTANYL CITRATE

Application Number

21947

Product Number

3

Dosage Form

-

Strength

EQ 0.4MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2006-09-25

Regulatory Status

Discontinued

2006
25 Sep
Discontinued Application: 21947

Drug Name

FENTORA

Product Number

4

Dosage Form

-

Strength

EQ 0.6MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2006-09-25

21947 / 4

Active Ingredient

FENTANYL CITRATE

Application Number

21947

Product Number

4

Dosage Form

-

Strength

EQ 0.6MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2006-09-25

Regulatory Status

Discontinued

2006
25 Sep
Discontinued Application: 21947

Drug Name

FENTORA

Product Number

5

Dosage Form

-

Strength

EQ 0.8MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2006-09-25

21947 / 5

Active Ingredient

FENTANYL CITRATE

Application Number

21947

Product Number

5

Dosage Form

-

Strength

EQ 0.8MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2006-09-25

Regulatory Status

Discontinued

2007
02 Mar
Discontinued Application: 21947

Drug Name

FENTORA

Product Number

6

Dosage Form

-

Strength

EQ 0.3MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2007-03-02

21947 / 6

Active Ingredient

FENTANYL CITRATE

Application Number

21947

Product Number

6

Dosage Form

-

Strength

EQ 0.3MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2007-03-02

Regulatory Status

Discontinued

1997
30 Sep
Discontinued Application: 20646

Drug Name

GABITRIL

Product Number

4

Dosage Form

-

Strength

20MG

Approval Date

1997-09-30

20646 / 4

Active Ingredient

TIAGABINE HYDROCHLORIDE

Application Number

20646

Product Number

4

Dosage Form

-

Strength

20MG

Approval Date

1997-09-30

Regulatory Status

Discontinued

2005
29 Nov
Discontinued Application: 20646

Drug Name

GABITRIL

Product Number

6

Dosage Form

-

Strength

6MG

Approval Date

2005-11-29

20646 / 6

Active Ingredient

TIAGABINE HYDROCHLORIDE

Application Number

20646

Product Number

6

Dosage Form

-

Strength

6MG

Approval Date

2005-11-29

Regulatory Status

Discontinued

2005
29 Nov
Discontinued Application: 20646

Drug Name

GABITRIL

Product Number

7

Dosage Form

-

Strength

8MG

Approval Date

2005-11-29

20646 / 7

Active Ingredient

TIAGABINE HYDROCHLORIDE

Application Number

20646

Product Number

7

Dosage Form

-

Strength

8MG

Approval Date

2005-11-29

Regulatory Status

Discontinued

2005
29 Nov
Discontinued Application: 20646

Drug Name

GABITRIL

Product Number

8

Dosage Form

-

Strength

10MG

Approval Date

2005-11-29

20646 / 8

Active Ingredient

TIAGABINE HYDROCHLORIDE

Application Number

20646

Product Number

8

Dosage Form

-

Strength

10MG

Approval Date

2005-11-29

Regulatory Status

Discontinued

2013
13 Sep
Discontinued Application: 22249

Drug Name

TREANDA

Product Number

3

Dosage Form

-

Strength

45MG/0.5ML (90MG/ML)

Approval Date

2013-09-13

22249 / 3

Active Ingredient

BENDAMUSTINE HYDROCHLORIDE

Application Number

22249

Product Number

3

Dosage Form

-

Strength

45MG/0.5ML (90MG/ML)

Approval Date

2013-09-13

Regulatory Status

Discontinued

2013
13 Sep
Discontinued Application: 22249

Drug Name

TREANDA

Product Number

4

Dosage Form

-

Strength

180MG/2ML (90MG/ML)

Approval Date

2013-09-13

22249 / 4

Active Ingredient

BENDAMUSTINE HYDROCHLORIDE

Application Number

22249

Product Number

4

Dosage Form

-

Strength

180MG/2ML (90MG/ML)

Approval Date

2013-09-13

Regulatory Status

Discontinued

2000
25 Sep
Discontinued Application: 21248

Drug Name

TRISENOX

Product Number

1

Dosage Form

-

Strength

1MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2000-09-25

21248 / 1

Active Ingredient

ARSENIC TRIOXIDE

Application Number

21248

Product Number

1

Dosage Form

-

Strength

1MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2000-09-25

Regulatory Status

Discontinued

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Drug Status Breakdown
23 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

ACTIQ

Application Number

20747

Product Number

1

Active Ingredient

FENTANYL CITRATE

Dosage Form

-

Strength

EQ 0.2MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

FDA Approved Drug Data

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