Lamisil - 0078-0179-05 - (terbinafine hydrochloride)

Alphabetical Index


Drug Information of Lamisil

Product NDC: 0078-0179
Proprietary Name: Lamisil
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 Lamisil

Product NDC: 0078-0179
Labeler Name: Novartis Pharmaceuticals Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020539
Marketing Category: NDA
Start Marketing Date: 19960510

Package Information of Lamisil

Package NDC: 0078-0179-05
Package Description: 100 TABLET in 1 BOTTLE (0078-0179-05)

NDC Information of Lamisil

NDC Code 0078-0179-05
Proprietary Name Lamisil
Package Description 100 TABLET in 1 BOTTLE (0078-0179-05)
Product NDC 0078-0179
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name terbinafine hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19960510
Marketing Category Name NDA
Labeler Name Novartis Pharmaceuticals Corporation
Substance Name TERBINAFINE HYDROCHLORIDE
Strength Number 250
Strength Unit mg/1
Pharmaceutical Classes Allylamine [Chemical/Ingredient],Allylamine Antifungal [EPC]

Complete Information of Lamisil


General Information