"50090-1624-2" National Drug Code (NDC)

NDC Code	50090-1624-2
Package Description	70 TABLET in 1 BOTTLE (50090-1624-2)
Product NDC	50090-1624
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Acyclovir
Non-Proprietary Name	Acyclovir
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20131129
Marketing Category Name	ANDA
Application Number	ANDA203834
Manufacturer	A-S Medication Solutions
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]