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terbinafine hydrochloride - 16714-501-01 - (terbinafine hydrochloride)

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Drug Information of terbinafine hydrochloride

Product NDC: 16714-501
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: 16714-501
Labeler Name: Northstar Rx LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078163
Marketing Category: ANDA
Start Marketing Date: 20090915

Package Information of terbinafine hydrochloride

Package NDC: 16714-501-01
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC (16714-501-01)

NDC Information of terbinafine hydrochloride

NDC Code 16714-501-01
Proprietary Name terbinafine hydrochloride
Package Description 30 TABLET in 1 BOTTLE, PLASTIC (16714-501-01)
Product NDC 16714-501
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name terbinafine hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090915
Marketing Category Name ANDA
Labeler Name Northstar Rx LLC
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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