Home > National Drug Code (NDC) > Famciclovir

Famciclovir - 0378-4491-05 - (famciclovir)

Alphabetical Index


Drug Information of Famciclovir

Product NDC: 0378-4491
Proprietary Name: Famciclovir
Non Proprietary Name: famciclovir
Active Ingredient(s): 250    mg/1 & nbsp;   famciclovir
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Famciclovir

Product NDC: 0378-4491
Labeler Name: Mylan Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA201333
Marketing Category: ANDA
Start Marketing Date: 20130522

Package Information of Famciclovir

Package NDC: 0378-4491-05
Package Description: 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-4491-05)

NDC Information of Famciclovir

NDC Code 0378-4491-05
Proprietary Name Famciclovir
Package Description 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-4491-05)
Product NDC 0378-4491
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name famciclovir
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20130522
Marketing Category Name ANDA
Labeler Name Mylan Pharmaceuticals Inc.
Substance Name FAMCICLOVIR
Strength Number 250
Strength Unit mg/1
Pharmaceutical Classes DNA Polymerase Inhibitors [MoA],Herpesvirus Nucleoside Analog DNA Polymerase Inhibitor [EPC],Nucleoside Analog [Chemical/Ingredient]

Complete Information of Famciclovir


General Information