"68788-0715-4" National Drug Code (NDC)

NDC Code	68788-0715-4
Package Description	473 mL in 1 BOTTLE (68788-0715-4)
Product NDC	68788-0715
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Acyclovir
Non-Proprietary Name	Acyclovir
Dosage Form	SUSPENSION
Usage	ORAL
Start Marketing Date	20110318
Marketing Category Name	ANDA
Application Number	ANDA077026
Manufacturer	Preferred Pharmaceuticals, Inc
Substance Name	ACYCLOVIR
Strength	200
Strength Unit	mg/5mL
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]