Astellas Pharma
FDA Approved Drugs

Astellas Pharma

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 Unclassified
  • Total Records 7
  • Latest Approval Date Nov 18, 2004
  • Data Source FDA
  • First Approval Date Jan 07, 1983
All
7
View
Unclassified
1
View
Discontinued
6
View
Company Overview

Company

Astellas Pharma

Country

Japan

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Company Snapshot

Astellas Pharma

2-5-1, Nihonbashi-Honcho, Chuo-Ku, Tokyo 103-8411

Japan

www.astellas.com/en/about View on Map
FDA Approved Drug Records ( 7 records )
1983
07 Jan
Discontinued Application: 18795

Drug Name

LOCOID

Product Number

1

Dosage Form

-

Strength

0.1%

Approval Date

1983-01-07

18795 / 1

Active Ingredient

HYDROCORTISONE BUTYRATE

Application Number

18795

Product Number

1

Dosage Form

-

Strength

0.1%

Approval Date

1983-01-07

Regulatory Status

Discontinued

1984
03 Jul
Discontinued Application: 19106

Drug Name

LOCOID

Product Number

1

Dosage Form

-

Strength

0.1%

Approval Date

1984-07-03

19106 / 1

Active Ingredient

HYDROCORTISONE BUTYRATE

Application Number

19106

Product Number

1

Dosage Form

-

Strength

0.1%

Approval Date

1984-07-03

Regulatory Status

Discontinued

1988
15 Sep
Discontinued Application: 19819

Drug Name

LOCOID

Product Number

1

Dosage Form

-

Strength

0.1%

Approval Date

1988-09-15

19819 / 1

Active Ingredient

HYDROCORTISONE BUTYRATE

Application Number

19819

Product Number

1

Dosage Form

-

Strength

0.1%

Approval Date

1988-09-15

Regulatory Status

Discontinued

-
Unclassified Application: 21754

Drug Name

MYCAMINE

Product Number

2

Dosage Form

-

Strength

50MG

Approval Date

-

21754 / 2

Active Ingredient

MICAFUNGIN SODIUM

Application Number

21754

Product Number

2

Dosage Form

-

Strength

50MG

Approval Date

-

Regulatory Status

Unclassified

2004
18 Nov
Discontinued Application: 21743

Drug Name

TARCEVA

Product Number

1

Dosage Form

-

Strength

EQ 25MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2004-11-18

21743 / 1

Active Ingredient

ERLOTINIB HYDROCHLORIDE

Application Number

21743

Product Number

1

Dosage Form

-

Strength

EQ 25MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2004-11-18

Regulatory Status

Discontinued

2004
18 Nov
Discontinued Application: 21743

Drug Name

TARCEVA

Product Number

2

Dosage Form

-

Strength

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

Approval Date

2004-11-18

21743 / 2

Active Ingredient

ERLOTINIB HYDROCHLORIDE

Application Number

21743

Product Number

2

Dosage Form

-

Strength

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

Approval Date

2004-11-18

Regulatory Status

Discontinued

2004
18 Nov
Discontinued Application: 21743

Drug Name

TARCEVA

Product Number

3

Dosage Form

-

Strength

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

Approval Date

2004-11-18

21743 / 3

Active Ingredient

ERLOTINIB HYDROCHLORIDE

Application Number

21743

Product Number

3

Dosage Form

-

Strength

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

Approval Date

2004-11-18

Regulatory Status

Discontinued

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Drug Status Breakdown
7 total
  • Discontinued
  • Unclassified
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

LOCOID

Application Number

18795

Product Number

1

Active Ingredient

HYDROCORTISONE BUTYRATE

Dosage Form

-

Strength

0.1%

FDA Approved Drug Data

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