"68788-7378-2" National Drug Code (NDC)

NDC Code	68788-7378-2
Package Description	21 TABLET in 1 BOTTLE (68788-7378-2)
Product NDC	68788-7378
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Acyclovir
Non-Proprietary Name	Acyclovir
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20160825
Marketing Category Name	ANDA
Application Number	ANDA204314
Manufacturer	Preferred Pharmaceuticals 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]