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Clemastine Fumarate - 0093-0308-01 - (Clemastine Fumarate)

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Drug Information of Clemastine Fumarate

Product NDC: 0093-0308
Proprietary Name: Clemastine Fumarate
Non Proprietary Name: Clemastine Fumarate
Active Ingredient(s): 2.68    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: 0093-0308
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA073283
Marketing Category: ANDA
Start Marketing Date: 19920401

Package Information of Clemastine Fumarate

Package NDC: 0093-0308-01
Package Description: 100 TABLET in 1 BOTTLE (0093-0308-01)

NDC Information of Clemastine Fumarate

NDC Code 0093-0308-01
Proprietary Name Clemastine Fumarate
Package Description 100 TABLET in 1 BOTTLE (0093-0308-01)
Product NDC 0093-0308
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Clemastine Fumarate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19920401
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA Inc
Substance Name CLEMASTINE FUMARATE
Strength Number 2.68
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Clemastine Fumarate


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