CEPHALON INC RX
FDA Approved Drugs

CEPHALON INC 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 7
  • Latest Approval Date Oct 13, 2017
  • Data Source FDA
  • First Approval Date Sep 30, 1997
All
31
View
Unclassified
1
View
Discontinued
23
View
RX
7
View
Company Overview

Company

CEPHALON INC RX

Country

U.S.A

Email

Social Profiles

Company Snapshot

CEPHALON INC RX

4745 Wiley Post Way Salt Lake City, UT 84116

U.S.A

www.tevapharm.com/ View on Map
FDA Approved Drug Records ( 7 records )
1997
30 Sep
RX Application: 20646

Drug Name

GABITRIL

Product Number

1

Dosage Form

-

Strength

4MG

Approval Date

1997-09-30

20646 / 1

Active Ingredient

TIAGABINE HYDROCHLORIDE

Application Number

20646

Product Number

1

Dosage Form

-

Strength

4MG

Approval Date

1997-09-30

Regulatory Status

RX

1997
30 Sep
RX Application: 20646

Drug Name

GABITRIL

Product Number

2

Dosage Form

-

Strength

12MG

Approval Date

1997-09-30

20646 / 2

Active Ingredient

TIAGABINE HYDROCHLORIDE

Application Number

20646

Product Number

2

Dosage Form

-

Strength

12MG

Approval Date

1997-09-30

Regulatory Status

RX

1997
30 Sep
RX Application: 20646

Drug Name

GABITRIL

Product Number

3

Dosage Form

-

Strength

16MG

Approval Date

1997-09-30

20646 / 3

Active Ingredient

TIAGABINE HYDROCHLORIDE

Application Number

20646

Product Number

3

Dosage Form

-

Strength

16MG

Approval Date

1997-09-30

Regulatory Status

RX

1999
16 Apr
RX Application: 20646

Drug Name

GABITRIL

Product Number

5

Dosage Form

-

Strength

2MG

Approval Date

1999-04-16

20646 / 5

Active Ingredient

TIAGABINE HYDROCHLORIDE

Application Number

20646

Product Number

5

Dosage Form

-

Strength

2MG

Approval Date

1999-04-16

Regulatory Status

RX

2008
20 Mar
RX Application: 22249

Drug Name

TREANDA

Product Number

1

Dosage Form

-

Strength

100MG/VIAL

Approval Date

2008-03-20

22249 / 1

Active Ingredient

BENDAMUSTINE HYDROCHLORIDE

Application Number

22249

Product Number

1

Dosage Form

-

Strength

100MG/VIAL

Approval Date

2008-03-20

Regulatory Status

RX

2009
01 May
RX Application: 22249

Drug Name

TREANDA

Product Number

2

Dosage Form

-

Strength

25MG/VIAL

Approval Date

2009-05-01

22249 / 2

Active Ingredient

BENDAMUSTINE HYDROCHLORIDE

Application Number

22249

Product Number

2

Dosage Form

-

Strength

25MG/VIAL

Approval Date

2009-05-01

Regulatory Status

RX

2017
13 Oct
RX Application: 21248

Drug Name

TRISENOX

Product Number

2

Dosage Form

-

Strength

2MG/ML

Approval Date

2017-10-13

21248 / 2

Active Ingredient

ARSENIC TRIOXIDE

Application Number

21248

Product Number

2

Dosage Form

-

Strength

2MG/ML

Approval Date

2017-10-13

Regulatory Status

RX

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Drug Status Breakdown
7 total
  • RX
Official Source

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

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FDA Approved Drug Record Details Preview

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

Drug Name

GABITRIL

Application Number

20646

Product Number

1

Active Ingredient

TIAGABINE HYDROCHLORIDE

Dosage Form

-

Strength

4MG

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