"63739-682-10" National Drug Code (NDC)

NDC Code	63739-682-10
Package Description	10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-682-10) > 10 TABLET in 1 BLISTER PACK
Product NDC	63739-682
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Acyclovir
Non-Proprietary Name	Acyclovir
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20091022
End Marketing Date	20201231
Marketing Category Name	ANDA
Application Number	ANDA075382
Manufacturer	McKesson Corporation dba SKY Packaging
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]