"0713-0630-15" National Drug Code (NDC)

NDC Code	0713-0630-15
Package Description	1 TUBE in 1 CARTON (0713-0630-15) > 15 g in 1 TUBE
Product NDC	0713-0630
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Acyclovir
Non-Proprietary Name	Acyclovir
Dosage Form	OINTMENT
Usage	TOPICAL
Start Marketing Date	20171113
End Marketing Date	20231031
Marketing Category Name	ANDA
Application Number	ANDA205591
Manufacturer	Cosette 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]