"68084-107-01" National Drug Code (NDC)

NDC Code	68084-107-01
Package Description	100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-107-01) / 1 CAPSULE in 1 BLISTER PACK (68084-107-11)
Product NDC	68084-107
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Acyclovir
Non-Proprietary Name	Acyclovir
Dosage Form	CAPSULE
Usage	ORAL
Start Marketing Date	20140206
End Marketing Date	20270430
Marketing Category Name	ANDA
Application Number	ANDA075677
Manufacturer	American Health Packaging
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]