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Terbinafine Hydrochloride - 51672-2080-1 - (Terbinafine Hydrochloride)

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Drug Information of Terbinafine Hydrochloride

Product NDC: 51672-2080
Proprietary Name: Terbinafine Hydrochloride
Non Proprietary Name: Terbinafine Hydrochloride
Active Ingredient(s): 1    g/100g & nbsp;   Terbinafine Hydrochloride
Administration Route(s): TOPICAL
Dosage Form(s): CREAM
Coding System: National Drug Codes(NDC)

Labeler Information of Terbinafine Hydrochloride

Product NDC: 51672-2080
Labeler Name: Taro Pharmaceuticals U.S.A., Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number: ANDA077511
Marketing Category: ANDA
Start Marketing Date: 20070702

Package Information of Terbinafine Hydrochloride

Package NDC: 51672-2080-1
Package Description: 1 TUBE in 1 CARTON (51672-2080-1) > 15 g in 1 TUBE

NDC Information of Terbinafine Hydrochloride

NDC Code 51672-2080-1
Proprietary Name Terbinafine Hydrochloride
Package Description 1 TUBE in 1 CARTON (51672-2080-1) > 15 g in 1 TUBE
Product NDC 51672-2080
Product Type Name HUMAN OTC DRUG
Non Proprietary Name Terbinafine Hydrochloride
Dosage Form Name CREAM
Route Name TOPICAL
Start Marketing Date 20070702
Marketing Category Name ANDA
Labeler Name Taro Pharmaceuticals U.S.A., Inc.
Substance Name TERBINAFINE HYDROCHLORIDE
Strength Number 1
Strength Unit g/100g
Pharmaceutical Classes

Complete Information of Terbinafine Hydrochloride


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