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TERBINAFINE HYDROCHLORIDE - 64679-743-05 - (TERBINAFINE HYDROCHLORIDE)

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Drug Information of TERBINAFINE HYDROCHLORIDE

Product NDC: 64679-743
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: 64679-743
Labeler Name: Wockhardt USA LLC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078229
Marketing Category: ANDA
Start Marketing Date: 20070702

Package Information of TERBINAFINE HYDROCHLORIDE

Package NDC: 64679-743-05
Package Description: 1 BLISTER PACK in 1 CARTON (64679-743-05) > 30 TABLET in 1 BLISTER PACK

NDC Information of TERBINAFINE HYDROCHLORIDE

NDC Code 64679-743-05
Proprietary Name TERBINAFINE HYDROCHLORIDE
Package Description 1 BLISTER PACK in 1 CARTON (64679-743-05) > 30 TABLET in 1 BLISTER PACK
Product NDC 64679-743
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 Wockhardt USA 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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