"60505-0042-6" National Drug Code (NDC)

NDC Code	60505-0042-6
Package Description	100 CAPSULE in 1 BOTTLE (60505-0042-6)
Product NDC	60505-0042
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Acyclovir
Non-Proprietary Name	Acyclovir
Dosage Form	CAPSULE
Usage	ORAL
Start Marketing Date	20060320
End Marketing Date	20270430
Marketing Category Name	ANDA
Application Number	ANDA075677
Manufacturer	Apotex Corp.
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]