Astellas Pharma Discontinued
FDA Approved Drugs

Astellas Pharma 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 Nov 18, 2004
  • Data Source FDA
  • First Approval Date Jan 07, 1983
All
7
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Unclassified
1
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Discontinued
6
View
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Astellas Pharma Discontinued

Country

Japan

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Company Snapshot

Astellas Pharma Discontinued

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

Japan

www.astellas.com/en/about View on Map
FDA Approved Drug Records ( 6 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

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EQ 25MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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EQ 25MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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
6 total
  • Discontinued
Official Source

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Drug Name

LOCOID

Application Number

18795

Product Number

1

Active Ingredient

HYDROCORTISONE BUTYRATE

Dosage Form

-

Strength

0.1%

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