Famvir - 0078-0366-15 - (famciclovir)

Alphabetical Index


Drug Information of Famvir

Product NDC: 0078-0366
Proprietary Name: Famvir
Non Proprietary Name: famciclovir
Active Ingredient(s): 125    mg/1 & nbsp;   famciclovir
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Famvir

Product NDC: 0078-0366
Labeler Name: Novartis Pharmaceuticals Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020363
Marketing Category: NDA
Start Marketing Date: 19940629

Package Information of Famvir

Package NDC: 0078-0366-15
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (0078-0366-15)

NDC Information of Famvir

NDC Code 0078-0366-15
Proprietary Name Famvir
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (0078-0366-15)
Product NDC 0078-0366
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name famciclovir
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19940629
Marketing Category Name NDA
Labeler Name Novartis Pharmaceuticals Corporation
Substance Name FAMCICLOVIR
Strength Number 125
Strength Unit mg/1
Pharmaceutical Classes DNA Polymerase Inhibitors [MoA],Herpesvirus Nucleoside Analog DNA Polymerase Inhibitor [EPC],Nucleoside Analog [Chemical/Ingredient]

Complete Information of Famvir


General Information