"16714-885-01" National Drug Code (NDC)

NDC Code	16714-885-01
Package Description	1 TUBE in 1 CARTON (16714-885-01) / 15 g in 1 TUBE
Product NDC	16714-885
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	Northstar Rx LLC
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]