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Terbinafine Hydrochloride - 67405-543-10 - (Terbinafine Hydrochloride)

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Drug Information of Terbinafine Hydrochloride

Product NDC: 67405-543
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: 67405-543
Labeler Name: Harris Pharmaceutical, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077919
Marketing Category: ANDA
Start Marketing Date: 20070730

Package Information of Terbinafine Hydrochloride

Package NDC: 67405-543-10
Package Description: 100 TABLET in 1 BOTTLE (67405-543-10)

NDC Information of Terbinafine Hydrochloride

NDC Code 67405-543-10
Proprietary Name Terbinafine Hydrochloride
Package Description 100 TABLET in 1 BOTTLE (67405-543-10)
Product NDC 67405-543
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Terbinafine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20070730
Marketing Category Name ANDA
Labeler Name Harris Pharmaceutical, 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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