Home > National Drug Code (NDC) > Terbinafine

Terbinafine - 65862-079-30 - (Terbinafine Hydrochloride)

Alphabetical Index


Drug Information of Terbinafine

Product NDC: 65862-079
Proprietary Name: Terbinafine
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

Product NDC: 65862-079
Labeler Name: Aurobindo Pharma Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078297
Marketing Category: ANDA
Start Marketing Date: 20070702

Package Information of Terbinafine

Package NDC: 65862-079-30
Package Description: 30 TABLET in 1 BOTTLE (65862-079-30)

NDC Information of Terbinafine

NDC Code 65862-079-30
Proprietary Name Terbinafine
Package Description 30 TABLET in 1 BOTTLE (65862-079-30)
Product NDC 65862-079
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 Aurobindo Pharma Limited
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