"42291-108-50" National Drug Code (NDC)

NDC Code	42291-108-50
Package Description	500 TABLET in 1 BOTTLE (42291-108-50)
Product NDC	42291-108
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Acyclovir
Non-Proprietary Name	Acyclovir
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	19990305
Marketing Category Name	ANDA
Application Number	ANDA075382
Manufacturer	AvKARE, Inc.
Substance Name	ACYCLOVIR
Strength	400
Strength Unit	mg/1
Pharmacy 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]