Aspen API
FDA Approved Drugs

Aspen API

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 10
  • Latest Approval Date Apr 27, 2007
  • Data Source FDA
  • First Approval Date Mar 24, 1999
Company Overview

Company

Aspen API

Country

Netherlands

Website

Visit Website

Email

api@nl.aspenpharma.com

Social Profiles

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Company Snapshot

Aspen API

Kloosterstraat 6, 5349 AB Oss

Netherlands

www.aspenapi.com/ api@nl.aspenpharma.com View on Map
FDA Approved Drug Records ( 10 records )
2002
21 Jun
Discontinued Application: 20992

Drug Name

CENESTIN

Product Number

1

Dosage Form

-

Strength

0.3MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2002-06-21

20992 / 1

Active Ingredient

ESTROGENS, CONJUGATED SYNTHETIC A

Application Number

20992

Product Number

1

Dosage Form

-

Strength

0.3MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2002-06-21

Regulatory Status

Discontinued

1999
24 Mar
Discontinued Application: 20992

Drug Name

CENESTIN

Product Number

2

Dosage Form

-

Strength

0.625MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1999-03-24

20992 / 2

Active Ingredient

ESTROGENS, CONJUGATED SYNTHETIC A

Application Number

20992

Product Number

2

Dosage Form

-

Strength

0.625MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1999-03-24

Regulatory Status

Discontinued

1999
24 Mar
Discontinued Application: 20992

Drug Name

CENESTIN

Product Number

3

Dosage Form

-

Strength

0.9MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1999-03-24

20992 / 3

Active Ingredient

ESTROGENS, CONJUGATED SYNTHETIC A

Application Number

20992

Product Number

3

Dosage Form

-

Strength

0.9MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1999-03-24

Regulatory Status

Discontinued

2000
13 Mar
Discontinued Application: 20992

Drug Name

CENESTIN

Product Number

4

Dosage Form

-

Strength

1.25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2000-03-13

20992 / 4

Active Ingredient

ESTROGENS, CONJUGATED SYNTHETIC A

Application Number

20992

Product Number

4

Dosage Form

-

Strength

1.25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2000-03-13

Regulatory Status

Discontinued

2004
05 Feb
Discontinued Application: 20992

Drug Name

CENESTIN

Product Number

5

Dosage Form

-

Strength

0.45MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2004-02-05

20992 / 5

Active Ingredient

ESTROGENS, CONJUGATED SYNTHETIC A

Application Number

20992

Product Number

5

Dosage Form

-

Strength

0.45MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2004-02-05

Regulatory Status

Discontinued

2004
20 Dec
Discontinued Application: 21443

Drug Name

ENJUVIA

Product Number

1

Dosage Form

-

Strength

0.3MG

Approval Date

2004-12-20

21443 / 1

Active Ingredient

ESTROGENS, CONJUGATED SYNTHETIC B

Application Number

21443

Product Number

1

Dosage Form

-

Strength

0.3MG

Approval Date

2004-12-20

Regulatory Status

Discontinued

2004
20 Dec
Discontinued Application: 21443

Drug Name

ENJUVIA

Product Number

2

Dosage Form

-

Strength

0.45MG

Approval Date

2004-12-20

21443 / 2

Active Ingredient

ESTROGENS, CONJUGATED SYNTHETIC B

Application Number

21443

Product Number

2

Dosage Form

-

Strength

0.45MG

Approval Date

2004-12-20

Regulatory Status

Discontinued

2004
10 May
Discontinued Application: 21443

Drug Name

ENJUVIA

Product Number

3

Dosage Form

-

Strength

0.625MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2004-05-10

21443 / 3

Active Ingredient

ESTROGENS, CONJUGATED SYNTHETIC B

Application Number

21443

Product Number

3

Dosage Form

-

Strength

0.625MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2004-05-10

Regulatory Status

Discontinued

2004
10 May
Discontinued Application: 21443

Drug Name

ENJUVIA

Product Number

4

Dosage Form

-

Strength

1.25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2004-05-10

21443 / 4

Active Ingredient

ESTROGENS, CONJUGATED SYNTHETIC B

Application Number

21443

Product Number

4

Dosage Form

-

Strength

1.25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

2004-05-10

Regulatory Status

Discontinued

2007
27 Apr
Discontinued Application: 21443

Drug Name

ENJUVIA

Product Number

5

Dosage Form

-

Strength

0.9MG

Approval Date

2007-04-27

21443 / 5

Active Ingredient

ESTROGENS, CONJUGATED SYNTHETIC B

Application Number

21443

Product Number

5

Dosage Form

-

Strength

0.9MG

Approval Date

2007-04-27

Regulatory Status

Discontinued

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Drug Status Breakdown
10 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

CENESTIN

Application Number

20992

Product Number

1

Active Ingredient

ESTROGENS, CONJUGATED SYNTHETIC A

Dosage Form

-

Strength

0.3MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

FDA Approved Drug Data

Approved drug product information

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