"68682-995-95" National Drug Code (NDC)

NDC Code	68682-995-95
Package Description	1 TUBE in 1 CARTON (68682-995-95) > 30 g in 1 TUBE
Product NDC	68682-995
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Acyclovir
Non-Proprietary Name	Acyclovir
Dosage Form	OINTMENT
Usage	TOPICAL
Start Marketing Date	20121003
End Marketing Date	20160630
Marketing Category Name	NDA AUTHORIZED GENERIC
Application Number	NDA018604
Manufacturer	Oceanside Pharmaceuticals
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 [Chemical/Ingredient]