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Terbinafine Hydrochloride - 21695-630-42 - (Terbinafine Hydrochloride)

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Drug Information of Terbinafine Hydrochloride

Product NDC: 21695-630
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: 21695-630
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077533
Marketing Category: ANDA
Start Marketing Date: 20070702

Package Information of Terbinafine Hydrochloride

Package NDC: 21695-630-42
Package Description: 42 TABLET in 1 BOTTLE (21695-630-42)

NDC Information of Terbinafine Hydrochloride

NDC Code 21695-630-42
Proprietary Name Terbinafine Hydrochloride
Package Description 42 TABLET in 1 BOTTLE (21695-630-42)
Product NDC 21695-630
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Terbinafine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20070702
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
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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