Home > National Drug Code (NDC) > Terbinafine

Terbinafine - 76282-209-30 - (Terbinafine)

Alphabetical Index


Drug Information of Terbinafine

Product NDC: 76282-209
Proprietary Name: Terbinafine
Non Proprietary Name: Terbinafine
Active Ingredient(s): 250    mg/1 & nbsp;   Terbinafine
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Terbinafine

Product NDC: 76282-209
Labeler Name: Exelan Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077533
Marketing Category: ANDA
Start Marketing Date: 20120425

Package Information of Terbinafine

Package NDC: 76282-209-30
Package Description: 30 TABLET in 1 BOTTLE (76282-209-30)

NDC Information of Terbinafine

NDC Code 76282-209-30
Proprietary Name Terbinafine
Package Description 30 TABLET in 1 BOTTLE (76282-209-30)
Product NDC 76282-209
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Terbinafine
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120425
Marketing Category Name ANDA
Labeler Name Exelan Pharmaceuticals Inc.
Substance Name TERBINAFINE HYDROCHLORIDE
Strength Number 250
Strength Unit mg/1
Pharmaceutical Classes Allylamine [Chemical/Ingredient],Allylamine Antifungal [EPC]

Complete Information of Terbinafine


General Information