Eisai Inc Discontinued
FDA Approved Drugs

Eisai 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 6
  • Latest Approval Date Dec 12, 2008
  • Data Source FDA
  • First Approval Date Dec 26, 1990
All
21
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Unclassified
4
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Discontinued
6
View
RX
11
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Company Overview

Company

Eisai Inc Discontinued

Country

U.S.A

Email

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Company Snapshot

Eisai Inc Discontinued

200 Metro Blvd, Nutley, NJ 07110

U.S.A

us.eisai.com/ View on Map
FDA Approved Drug Records ( 6 records )
2004
18 Oct
Discontinued Application: 21719

Drug Name

ARICEPT

Product Number

1

Dosage Form

-

Strength

5MG/5ML

Approval Date

2004-10-18

21719 / 1

Active Ingredient

DONEPEZIL HYDROCHLORIDE

Application Number

21719

Product Number

1

Dosage Form

-

Strength

5MG/5ML

Approval Date

2004-10-18

Regulatory Status

Discontinued

2004
18 Oct
Discontinued Application: 21720

Drug Name

ARICEPT ODT

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2004-10-18

21720 / 1

Active Ingredient

DONEPEZIL HYDROCHLORIDE

Application Number

21720

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2004-10-18

Regulatory Status

Discontinued

2004
18 Oct
Discontinued Application: 21720

Drug Name

ARICEPT ODT

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

2004-10-18

21720 / 2

Active Ingredient

DONEPEZIL HYDROCHLORIDE

Application Number

21720

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

2004-10-18

Regulatory Status

Discontinued

2008
14 Nov
Discontinued Application: 21911

Drug Name

BANZEL

Product Number

1

Dosage Form

-

Strength

100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2008-11-14

21911 / 1

Active Ingredient

RUFINAMIDE

Application Number

21911

Product Number

1

Dosage Form

-

Strength

100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2008-11-14

Regulatory Status

Discontinued

1990
26 Dec
Discontinued Application: 19926

Drug Name

HEXALEN

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1990-12-26

19926 / 1

Active Ingredient

ALTRETAMINE

Application Number

19926

Product Number

1

Dosage Form

-

Strength

50MG

Approval Date

1990-12-26

Regulatory Status

Discontinued

2008
12 Dec
Discontinued Application: 22244

Drug Name

LUSEDRA

Product Number

1

Dosage Form

-

Strength

1050MG/30ML (35MG/ML)

Approval Date

2008-12-12

22244 / 1

Active Ingredient

FOSPROPOFOL DISODIUM

Application Number

22244

Product Number

1

Dosage Form

-

Strength

1050MG/30ML (35MG/ML)

Approval Date

2008-12-12

Regulatory Status

Discontinued

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Drug Status Breakdown
6 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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FDA Approved Drug Record Details Preview

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

Drug Name

ARICEPT

Application Number

21719

Product Number

1

Active Ingredient

DONEPEZIL HYDROCHLORIDE

Dosage Form

-

Strength

5MG/5ML

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