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Famciclovir - 0054-0196-13 - (Famciclovir)

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Drug Information of Famciclovir

Product NDC: 0054-0196
Proprietary Name: Famciclovir
Non Proprietary Name: Famciclovir
Active Ingredient(s): 125    mg/1 & nbsp;   Famciclovir
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Famciclovir

Product NDC: 0054-0196
Labeler Name: Roxane Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090128
Marketing Category: ANDA
Start Marketing Date: 20110103

Package Information of Famciclovir

Package NDC: 0054-0196-13
Package Description: 30 TABLET in 1 BOTTLE (0054-0196-13)

NDC Information of Famciclovir

NDC Code 0054-0196-13
Proprietary Name Famciclovir
Package Description 30 TABLET in 1 BOTTLE (0054-0196-13)
Product NDC 0054-0196
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Famciclovir
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110103
Marketing Category Name ANDA
Labeler Name Roxane Laboratories, Inc.
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 Famciclovir


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