"50090-6561-0" National Drug Code (NDC)

NDC Code	50090-6561-0
Package Description	1 TUBE in 1 CARTON (50090-6561-0) / 15 g in 1 TUBE
Product NDC	50090-6561
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Acyclovir
Non-Proprietary Name	Acyclovir
Dosage Form	OINTMENT
Usage	TOPICAL
Start Marketing Date	20170731
Marketing Category Name	ANDA
Application Number	ANDA205510
Manufacturer	A-S Medication Solutions
Substance Name	ACYCLOVIR
Strength	50
Strength Unit	mg/g
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]