"51655-099-51" National Drug Code (NDC)

NDC Code	51655-099-51
Package Description	40 TABLET in 1 BOTTLE, DISPENSING (51655-099-51)
Product NDC	51655-099
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Acyclovir
Non-Proprietary Name	Acyclovir
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20140514
Marketing Category Name	ANDA
Application Number	ANDA075382
Manufacturer	Northwind Pharmaceuticals
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]