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Famciclovir - 0093-8119-56 - (Famciclovir)

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Drug Information of Famciclovir

Product NDC: 0093-8119
Proprietary Name: Famciclovir
Non Proprietary Name: Famciclovir
Active Ingredient(s): 500    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: 0093-8119
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077487
Marketing Category: ANDA
Start Marketing Date: 20070905

Package Information of Famciclovir

Package NDC: 0093-8119-56
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (0093-8119-56)

NDC Information of Famciclovir

NDC Code 0093-8119-56
Proprietary Name Famciclovir
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (0093-8119-56)
Product NDC 0093-8119
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Famciclovir
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20070905
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA Inc
Substance Name FAMCICLOVIR
Strength Number 500
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


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