"68382-792-30" National Drug Code (NDC)

NDC Code	68382-792-30
Package Description	10 BLISTER PACK in 1 CARTON (68382-792-30) / 10 TABLET in 1 BLISTER PACK
Product NDC	68382-792
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Acyclovir
Non-Proprietary Name	Acyclovir
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20140910
Marketing Category Name	ANDA
Application Number	ANDA204314
Manufacturer	Zydus Pharmaceuticals (USA) Inc.
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]