Genus Lifesciences Discontinued
FDA Approved Drugs

Genus Lifesciences 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 Sep 14, 2016
  • Data Source FDA
  • First Approval Date May 15, 2003
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Discontinued
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RX
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Company Overview

Company

Genus Lifesciences Discontinued

Country

U.S.A

Social Profiles

Company Snapshot

Genus Lifesciences Discontinued

514 North 12th Street, Allentown, PA 18102

U.S.A

genuslifesciences.com/ iInfo@GenusLifesciences.com View on Map
FDA Approved Drug Records ( 4 records )
2003
15 May
Discontinued Application: 76065

Drug Name

AMCINONIDE

Product Number

1

Dosage Form

-

Strength

0.1%

Approval Date

2003-05-15

76065 / 1

Active Ingredient

AMCINONIDE

Application Number

76065

Product Number

1

Dosage Form

-

Strength

0.1%

Approval Date

2003-05-15

Regulatory Status

Discontinued

2008
08 Feb
Discontinued Application: 40613

Drug Name

HYDROCODONE BITARTRATE AND HOMATROPINE METHYLBROMIDE

Product Number

1

Dosage Form

-

Strength

1.5MG/5ML;5MG/5ML

Approval Date

2008-02-08

40613 / 1

Active Ingredient

HOMATROPINE METHYLBROMIDE; HYDROCODONE BITARTRATE

Application Number

40613

Product Number

1

Dosage Form

-

Strength

1.5MG/5ML;5MG/5ML

Approval Date

2008-02-08

Regulatory Status

Discontinued

2016
14 Sep
Discontinued Application: 205103

Drug Name

YOSPRALA

Product Number

1

Dosage Form

-

Strength

81MG;40MG

Approval Date

2016-09-14

205103 / 1

Active Ingredient

ASPIRIN; OMEPRAZOLE

Application Number

205103

Product Number

1

Dosage Form

-

Strength

81MG;40MG

Approval Date

2016-09-14

Regulatory Status

Discontinued

2016
14 Sep
Discontinued Application: 205103

Drug Name

YOSPRALA

Product Number

2

Dosage Form

-

Strength

325MG;40MG

Approval Date

2016-09-14

205103 / 2

Active Ingredient

ASPIRIN; OMEPRAZOLE

Application Number

205103

Product Number

2

Dosage Form

-

Strength

325MG;40MG

Approval Date

2016-09-14

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

AMCINONIDE

Application Number

76065

Product Number

1

Active Ingredient

AMCINONIDE

Dosage Form

-

Strength

0.1%

FDA Approved Drug Data

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