"68071-2488-3" National Drug Code (NDC)

NDC Code	68071-2488-3
Package Description	1 TUBE in 1 CARTON (68071-2488-3) > 30 g in 1 TUBE
Product NDC	68071-2488
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Acyclovir
Non-Proprietary Name	Acyclovir
Dosage Form	OINTMENT
Usage	TOPICAL
Start Marketing Date	20200608
Marketing Category Name	ANDA
Application Number	ANDA205974
Manufacturer	NuCare Pharmaceuticals,Inc.
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]