Haleon Discontinued
FDA Approved Drugs

Haleon 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 4
  • Latest Approval Date Jan 30, 1998
  • Data Source FDA
  • First Approval Date Sep 19, 1989
All
42
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Discontinued
4
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OTC
38
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Company

Haleon Discontinued

Country

United Kingdom

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Company Snapshot

Haleon Discontinued

Building 5, First Floor the Heights Weybridge Surrey KT13 0NY

United Kingdom

www.haleon.com/ View on Map
FDA Approved Drug Records ( 4 records )
1989
19 Sep
Discontinued Application: 19833

Drug Name

CHILDRENS ADVIL

Product Number

2

Dosage Form

-

Strength

100MG/5ML

Approval Date

1989-09-19

19833 / 2

Active Ingredient

IBUPROFEN

Application Number

19833

Product Number

2

Dosage Form

-

Strength

100MG/5ML

Approval Date

1989-09-19

Regulatory Status

Discontinued

1994
19 Oct
Discontinued Application: 20121

Drug Name

FLONASE

Product Number

1

Dosage Form

-

Strength

0.05MG/SPRAY **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1994-10-19

20121 / 1

Active Ingredient

FLUTICASONE PROPIONATE

Application Number

20121

Product Number

1

Dosage Form

-

Strength

0.05MG/SPRAY **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1994-10-19

Regulatory Status

Discontinued

1998
30 Jan
Discontinued Application: 20812

Drug Name

PEDIATRIC ADVIL

Product Number

1

Dosage Form

-

Strength

100MG/2.5ML

Approval Date

1998-01-30

20812 / 1

Active Ingredient

IBUPROFEN

Application Number

20812

Product Number

1

Dosage Form

-

Strength

100MG/2.5ML

Approval Date

1998-01-30

Regulatory Status

Discontinued

1992
21 Aug
Discontinued Application: 20925

Drug Name

TAVIST-1

Product Number

1

Dosage Form

-

Strength

1.34MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1992-08-21

20925 / 1

Active Ingredient

CLEMASTINE FUMARATE

Application Number

20925

Product Number

1

Dosage Form

-

Strength

1.34MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date

1992-08-21

Regulatory Status

Discontinued

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Drug Status Breakdown
4 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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Explore important FDA approved drug information available in the records above.

Drug Name

CHILDRENS ADVIL

Application Number

19833

Product Number

2

Active Ingredient

IBUPROFEN

Dosage Form

-

Strength

100MG/5ML

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