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Famciclovir - 16714-304-01 - (Famciclovir)

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Drug Information of Famciclovir

Product NDC: 16714-304
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: 16714-304
Labeler Name: NorthStar Rx LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091114
Marketing Category: ANDA
Start Marketing Date: 20110321

Package Information of Famciclovir

Package NDC: 16714-304-01
Package Description: 30 TABLET, FILM COATED in 1 BOTTLE (16714-304-01)

NDC Information of Famciclovir

NDC Code 16714-304-01
Proprietary Name Famciclovir
Package Description 30 TABLET, FILM COATED in 1 BOTTLE (16714-304-01)
Product NDC 16714-304
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Famciclovir
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20110321
Marketing Category Name ANDA
Labeler Name NorthStar Rx LLC
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


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