"16590-003-25" National Drug Code (NDC)

NDC Code	16590-003-25
Package Description	25 TABLET in 1 BOTTLE (16590-003-25)
Product NDC	16590-003
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Acyclovir
Non-Proprietary Name	Acyclovir
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	19980930
Marketing Category Name	ANDA
Application Number	ANDA074980
Manufacturer	Stat Rx USA
Substance Name	ACYCLOVIR
Strength	800
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]