"55289-629-20" National Drug Code (NDC)

NDC Code	55289-629-20
Package Description	20 TABLET in 1 BOTTLE, PLASTIC (55289-629-20)
Product NDC	55289-629
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Acyclovir
Non-Proprietary Name	Acyclovir
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	19970430
Marketing Category Name	ANDA
Application Number	ANDA074556
Manufacturer	PD-Rx Pharmaceuticals, Inc.
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 [EXT]