"43063-340-05" National Drug Code (NDC)

NDC Code	43063-340-05
Package Description	5 TABLET in 1 BOTTLE, PLASTIC (43063-340-05)
Product NDC	43063-340
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Acyclovir
Non-Proprietary Name	Acyclovir
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20091022
Marketing Category Name	ANDA
Application Number	ANDA075382
Manufacturer	PD-Rx Pharmaceuticals, 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 [EXT]