"0093-3630-20" National Drug Code (NDC)

NDC Code	0093-3630-20
Package Description	1 TUBE in 1 CARTON (0093-3630-20) / 5 g in 1 TUBE
Product NDC	0093-3630
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Acyclovir
Non-Proprietary Name	Acyclovir
Dosage Form	CREAM
Usage	TOPICAL
Start Marketing Date	20190829
Marketing Category Name	NDA AUTHORIZED GENERIC
Application Number	NDA021478
Manufacturer	Teva Pharmaceuticals USA, 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]