"43063-701-35" National Drug Code (NDC)

NDC Code	43063-701-35
Package Description	35 CAPSULE in 1 BOTTLE, PLASTIC (43063-701-35)
Product NDC	43063-701
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Acyclovir
Non-Proprietary Name	Acyclovir
Dosage Form	CAPSULE
Usage	ORAL
Start Marketing Date	20150201
Marketing Category Name	ANDA
Application Number	ANDA075090
Manufacturer	PD-Rx Pharmaceuticals, Inc.
Substance Name	ACYCLOVIR
Strength	200
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]