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Clemastine Fumarate - 54868-5913-0 - (Clemastine Fumarate)

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Drug Information of Clemastine Fumarate

Product NDC: 54868-5913
Proprietary Name: Clemastine Fumarate
Non Proprietary Name: Clemastine Fumarate
Active Ingredient(s): 1.34    mg/1 & nbsp;   Clemastine Fumarate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Clemastine Fumarate

Product NDC: 54868-5913
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA073458
Marketing Category: ANDA
Start Marketing Date: 20080627

Package Information of Clemastine Fumarate

Package NDC: 54868-5913-0
Package Description: 100 TABLET in 1 BOTTLE (54868-5913-0)

NDC Information of Clemastine Fumarate

NDC Code 54868-5913-0
Proprietary Name Clemastine Fumarate
Package Description 100 TABLET in 1 BOTTLE (54868-5913-0)
Product NDC 54868-5913
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Clemastine Fumarate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20080627
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name CLEMASTINE FUMARATE
Strength Number 1.34
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Clemastine Fumarate


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