Wyeth Pharmaceuticals Inc RX
FDA Approved Drugs

Wyeth Pharmaceuticals 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 17
  • Latest Approval Date Oct 03, 2013
  • Data Source FDA
  • First Approval Date Jan 01, 1982
All
73
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Unclassified
4
View
Discontinued
52
View
RX
17
View
Company Overview

Company

Wyeth Pharmaceuticals Inc RX

Country

U.S.A

Website

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Company Snapshot

Wyeth Pharmaceuticals Inc RX

500 Arcola Road Collegeville, PA 19426

U.S.A

www.wyeth.com View on Map
FDA Approved Drug Records ( 17 records )
2013
03 Oct
RX Application: 22247

Drug Name

DUAVEE

Product Number

1

Dosage Form

-

Strength

EQ 20MG BASE;0.45MG

Approval Date

2013-10-03

22247 / 1

Active Ingredient

BAZEDOXIFENE ACETATE; ESTROGENS, CONJUGATED

Application Number

22247

Product Number

1

Dosage Form

-

Strength

EQ 20MG BASE;0.45MG

Approval Date

2013-10-03

Regulatory Status

RX

1982
01 Jan
RX Application: 4782

Drug Name

PREMARIN

Product Number

1

Dosage Form

-

Strength

1.25MG

Approval Date

1982-01-01

4782 / 1

Active Ingredient

ESTROGENS, CONJUGATED

Application Number

4782

Product Number

1

Dosage Form

-

Strength

1.25MG

Approval Date

1982-01-01

Regulatory Status

RX

1982
01 Jan
RX Application: 4782

Drug Name

PREMARIN

Product Number

3

Dosage Form

-

Strength

0.3MG

Approval Date

1982-01-01

4782 / 3

Active Ingredient

ESTROGENS, CONJUGATED

Application Number

4782

Product Number

3

Dosage Form

-

Strength

0.3MG

Approval Date

1982-01-01

Regulatory Status

RX

1982
01 Jan
RX Application: 4782

Drug Name

PREMARIN

Product Number

4

Dosage Form

-

Strength

0.625MG

Approval Date

1982-01-01

4782 / 4

Active Ingredient

ESTROGENS, CONJUGATED

Application Number

4782

Product Number

4

Dosage Form

-

Strength

0.625MG

Approval Date

1982-01-01

Regulatory Status

RX

1984
26 Jan
RX Application: 4782

Drug Name

PREMARIN

Product Number

5

Dosage Form

-

Strength

0.9MG

Approval Date

1984-01-26

4782 / 5

Active Ingredient

ESTROGENS, CONJUGATED

Application Number

4782

Product Number

5

Dosage Form

-

Strength

0.9MG

Approval Date

1984-01-26

Regulatory Status

RX

2003
16 Jul
RX Application: 4782

Drug Name

PREMARIN

Product Number

6

Dosage Form

-

Strength

0.45MG

Approval Date

2003-07-16

4782 / 6

Active Ingredient

ESTROGENS, CONJUGATED

Application Number

4782

Product Number

6

Dosage Form

-

Strength

0.45MG

Approval Date

2003-07-16

Regulatory Status

RX

1982
01 Jan
RX Application: 10402

Drug Name

PREMARIN

Product Number

1

Dosage Form

-

Strength

25MG/VIAL

Approval Date

1982-01-01

10402 / 1

Active Ingredient

ESTROGENS, CONJUGATED

Application Number

10402

Product Number

1

Dosage Form

-

Strength

25MG/VIAL

Approval Date

1982-01-01

Regulatory Status

RX

1982
01 Jan
RX Application: 20216

Drug Name

PREMARIN

Product Number

1

Dosage Form

-

Strength

0.625MG/GM

Approval Date

1982-01-01

20216 / 1

Active Ingredient

ESTROGENS, CONJUGATED

Application Number

20216

Product Number

1

Dosage Form

-

Strength

0.625MG/GM

Approval Date

1982-01-01

Regulatory Status

RX

1995
17 Nov
RX Application: 20527

Drug Name

PREMPHASE 14/14

Product Number

2

Dosage Form

-

Strength

0.625MG,0.625MG;N/A,5MG

Approval Date

1995-11-17

20527 / 2

Active Ingredient

ESTROGENS, CONJUGATED; MEDROXYPROGESTERONE ACETATE

Application Number

20527

Product Number

2

Dosage Form

-

Strength

0.625MG,0.625MG;N/A,5MG

Approval Date

1995-11-17

Regulatory Status

RX

1995
17 Nov
RX Application: 20527

Drug Name

PREMPRO

Product Number

1

Dosage Form

-

Strength

0.625MG;2.5MG

Approval Date

1995-11-17

20527 / 1

Active Ingredient

ESTROGENS, CONJUGATED; MEDROXYPROGESTERONE ACETATE

Application Number

20527

Product Number

1

Dosage Form

-

Strength

0.625MG;2.5MG

Approval Date

1995-11-17

Regulatory Status

RX

1998
09 Jan
RX Application: 20527

Drug Name

PREMPRO

Product Number

3

Dosage Form

-

Strength

0.625MG;5MG

Approval Date

1998-01-09

20527 / 3

Active Ingredient

ESTROGENS, CONJUGATED; MEDROXYPROGESTERONE ACETATE

Application Number

20527

Product Number

3

Dosage Form

-

Strength

0.625MG;5MG

Approval Date

1998-01-09

Regulatory Status

RX

2003
12 Mar
RX Application: 20527

Drug Name

PREMPRO

Product Number

4

Dosage Form

-

Strength

0.45MG;1.5MG

Approval Date

2003-03-12

20527 / 4

Active Ingredient

ESTROGENS, CONJUGATED; MEDROXYPROGESTERONE ACETATE

Application Number

20527

Product Number

4

Dosage Form

-

Strength

0.45MG;1.5MG

Approval Date

2003-03-12

Regulatory Status

RX

2003
04 Jun
RX Application: 20527

Drug Name

PREMPRO

Product Number

5

Dosage Form

-

Strength

0.3MG;1.5MG

Approval Date

2003-06-04

20527 / 5

Active Ingredient

ESTROGENS, CONJUGATED; MEDROXYPROGESTERONE ACETATE

Application Number

20527

Product Number

5

Dosage Form

-

Strength

0.3MG;1.5MG

Approval Date

2003-06-04

Regulatory Status

RX

2000
02 Feb
RX Application: 20987

Drug Name

PROTONIX

Product Number

1

Dosage Form

-

Strength

EQ 40MG BASE

Approval Date

2000-02-02

20987 / 1

Active Ingredient

PANTOPRAZOLE SODIUM

Application Number

20987

Product Number

1

Dosage Form

-

Strength

EQ 40MG BASE

Approval Date

2000-02-02

Regulatory Status

RX

2001
12 Jun
RX Application: 20987

Drug Name

PROTONIX

Product Number

2

Dosage Form

-

Strength

EQ 20MG BASE

Approval Date

2001-06-12

20987 / 2

Active Ingredient

PANTOPRAZOLE SODIUM

Application Number

20987

Product Number

2

Dosage Form

-

Strength

EQ 20MG BASE

Approval Date

2001-06-12

Regulatory Status

RX

2007
14 Nov
RX Application: 22020

Drug Name

PROTONIX

Product Number

1

Dosage Form

-

Strength

EQ 40MG BASE

Approval Date

2007-11-14

22020 / 1

Active Ingredient

PANTOPRAZOLE SODIUM

Application Number

22020

Product Number

1

Dosage Form

-

Strength

EQ 40MG BASE

Approval Date

2007-11-14

Regulatory Status

RX

2001
22 Mar
RX Application: 20988

Drug Name

PROTONIX IV

Product Number

1

Dosage Form

-

Strength

EQ 40MG BASE/VIAL

Approval Date

2001-03-22

20988 / 1

Active Ingredient

PANTOPRAZOLE SODIUM

Application Number

20988

Product Number

1

Dosage Form

-

Strength

EQ 40MG BASE/VIAL

Approval Date

2001-03-22

Regulatory Status

RX

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Drug Status Breakdown
17 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

DUAVEE

Application Number

22247

Product Number

1

Active Ingredient

BAZEDOXIFENE ACETATE; ESTROGENS, CONJUGATED

Dosage Form

-

Strength

EQ 20MG BASE;0.45MG

FDA Approved Drug Data

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