"68788-4142-1" National Drug Code (NDC)

NDC Code	68788-4142-1
Package Description	15 g in 1 TUBE (68788-4142-1)
Product NDC	68788-4142
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Acyclovir
Non-Proprietary Name	Acyclovir
Dosage Form	OINTMENT
Usage	TOPICAL
Start Marketing Date	20260812
Marketing Category Name	ANDA
Application Number	ANDA209971
Manufacturer	c
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]