"68084-109-01" National Drug Code (NDC)

NDC Code	68084-109-01
Package Description	100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-109-01) / 1 TABLET in 1 BLISTER PACK (68084-109-11)
Product NDC	68084-109
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Acyclovir
Non-Proprietary Name	Acyclovir
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20140206
End Marketing Date	20251231
Marketing Category Name	ANDA
Application Number	ANDA077309
Manufacturer	American Health Packaging
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]