Eisai Inc RX
FDA Approved Drugs

Eisai 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 11
  • Latest Approval Date Apr 07, 2020
  • Data Source FDA
  • First Approval Date Nov 25, 1996
All
21
View
Unclassified
4
View
Discontinued
6
View
RX
11
View
Company Overview

Company

Eisai Inc RX

Country

U.S.A

Website

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Company Snapshot

Eisai Inc RX

200 Metro Blvd, Nutley, NJ 07110

U.S.A

us.eisai.com/ View on Map
FDA Approved Drug Records ( 11 records )
1996
25 Nov
RX Application: 20690

Drug Name

ARICEPT

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1996-11-25

20690 / 1

Active Ingredient

DONEPEZIL HYDROCHLORIDE

Application Number

20690

Product Number

1

Dosage Form

-

Strength

10MG

Approval Date

1996-11-25

Regulatory Status

RX

1996
25 Nov
RX Application: 20690

Drug Name

ARICEPT

Product Number

2

Dosage Form

-

Strength

5MG

Approval Date

1996-11-25

20690 / 2

Active Ingredient

DONEPEZIL HYDROCHLORIDE

Application Number

20690

Product Number

2

Dosage Form

-

Strength

5MG

Approval Date

1996-11-25

Regulatory Status

RX

2010
23 Jul
RX Application: 22568

Drug Name

ARICEPT

Product Number

1

Dosage Form

-

Strength

23MG

Approval Date

2010-07-23

22568 / 1

Active Ingredient

DONEPEZIL HYDROCHLORIDE

Application Number

22568

Product Number

1

Dosage Form

-

Strength

23MG

Approval Date

2010-07-23

Regulatory Status

RX

2008
14 Nov
RX Application: 21911

Drug Name

BANZEL

Product Number

2

Dosage Form

-

Strength

200MG

Approval Date

2008-11-14

21911 / 2

Active Ingredient

RUFINAMIDE

Application Number

21911

Product Number

2

Dosage Form

-

Strength

200MG

Approval Date

2008-11-14

Regulatory Status

RX

2008
14 Nov
RX Application: 21911

Drug Name

BANZEL

Product Number

3

Dosage Form

-

Strength

400MG

Approval Date

2008-11-14

21911 / 3

Active Ingredient

RUFINAMIDE

Application Number

21911

Product Number

3

Dosage Form

-

Strength

400MG

Approval Date

2008-11-14

Regulatory Status

RX

2011
03 Mar
RX Application: 201367

Drug Name

BANZEL

Product Number

1

Dosage Form

-

Strength

40MG/ML

Approval Date

2011-03-03

201367 / 1

Active Ingredient

RUFINAMIDE

Application Number

201367

Product Number

1

Dosage Form

-

Strength

40MG/ML

Approval Date

2011-03-03

Regulatory Status

RX

2020
07 Apr
RX Application: 212028

Drug Name

DAYVIGO

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2020-04-07

212028 / 1

Active Ingredient

LEMBOREXANT

Application Number

212028

Product Number

1

Dosage Form

-

Strength

5MG

Approval Date

2020-04-07

Regulatory Status

RX

2020
07 Apr
RX Application: 212028

Drug Name

DAYVIGO

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

2020-04-07

212028 / 2

Active Ingredient

LEMBOREXANT

Application Number

212028

Product Number

2

Dosage Form

-

Strength

10MG

Approval Date

2020-04-07

Regulatory Status

RX

2010
15 Nov
RX Application: 201532

Drug Name

HALAVEN

Product Number

1

Dosage Form

-

Strength

1MG/2ML (0.5MG/ML)

Approval Date

2010-11-15

201532 / 1

Active Ingredient

ERIBULIN MESYLATE

Application Number

201532

Product Number

1

Dosage Form

-

Strength

1MG/2ML (0.5MG/ML)

Approval Date

2010-11-15

Regulatory Status

RX

2015
13 Feb
RX Application: 206947

Drug Name

LENVIMA

Product Number

1

Dosage Form

-

Strength

EQ 4MG BASE

Approval Date

2015-02-13

206947 / 1

Active Ingredient

LENVATINIB MESYLATE

Application Number

206947

Product Number

1

Dosage Form

-

Strength

EQ 4MG BASE

Approval Date

2015-02-13

Regulatory Status

RX

2015
13 Feb
RX Application: 206947

Drug Name

LENVIMA

Product Number

2

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

2015-02-13

206947 / 2

Active Ingredient

LENVATINIB MESYLATE

Application Number

206947

Product Number

2

Dosage Form

-

Strength

EQ 10MG BASE

Approval Date

2015-02-13

Regulatory Status

RX

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Drug Status Breakdown
11 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

ARICEPT

Application Number

20690

Product Number

1

Active Ingredient

DONEPEZIL HYDROCHLORIDE

Dosage Form

-

Strength

10MG

FDA Approved Drug Data

Approved drug product information

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