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Terbinafine Hydrochloride - 0093-7294-56 - (Terbinafine Hydrochloride)

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Drug Information of Terbinafine Hydrochloride

Product NDC: 0093-7294
Proprietary Name: Terbinafine Hydrochloride
Non Proprietary Name: Terbinafine Hydrochloride
Active Ingredient(s): 250    mg/1 & nbsp;   Terbinafine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Terbinafine Hydrochloride

Product NDC: 0093-7294
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076377
Marketing Category: ANDA
Start Marketing Date: 20070703

Package Information of Terbinafine Hydrochloride

Package NDC: 0093-7294-56
Package Description: 30 TABLET in 1 BOTTLE (0093-7294-56)

NDC Information of Terbinafine Hydrochloride

NDC Code 0093-7294-56
Proprietary Name Terbinafine Hydrochloride
Package Description 30 TABLET in 1 BOTTLE (0093-7294-56)
Product NDC 0093-7294
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Terbinafine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20070703
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA Inc
Substance Name TERBINAFINE HYDROCHLORIDE
Strength Number 250
Strength Unit mg/1
Pharmaceutical Classes Allylamine [Chemical/Ingredient],Allylamine Antifungal [EPC]

Complete Information of Terbinafine Hydrochloride


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