Acyclovir - 63629-1678-3 - (Acyclovir)

Alphabetical Index


Drug Information of Acyclovir

Product NDC: 63629-1678
Proprietary Name: Acyclovir
Non Proprietary Name: Acyclovir
Active Ingredient(s): 800    mg/1 & nbsp;   Acyclovir
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Acyclovir

Product NDC: 63629-1678
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075382
Marketing Category: ANDA
Start Marketing Date: 19990305

Package Information of Acyclovir

Package NDC: 63629-1678-3
Package Description: 30 TABLET in 1 BOTTLE (63629-1678-3)

NDC Information of Acyclovir

NDC Code 63629-1678-3
Proprietary Name Acyclovir
Package Description 30 TABLET in 1 BOTTLE (63629-1678-3)
Product NDC 63629-1678
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Acyclovir
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19990305
Marketing Category Name ANDA
Labeler Name Bryant Ranch Prepack
Substance Name ACYCLOVIR
Strength Number 800
Strength Unit mg/1
Pharmaceutical Classes DNA Polymerase Inhibitors [MoA],Herpes Simplex Virus Nucleoside Analog DNA Polymerase Inhibitor [EPC],Herpes Zoster Virus Nucleoside Analog DNA Polymerase Inhibitor [EPC],Herpesvirus Nucleoside Analog DNA Polymerase Inhibitor [EPC],Nucleoside Analog [Chemical/Ingredient]

Complete Information of Acyclovir


General Information