"67046-1031-3" National Drug Code (NDC)

NDC Code	67046-1031-3
Package Description	30 CAPSULE in 1 BLISTER PACK (67046-1031-3)
Product NDC	67046-1031
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Acyclovir
Non-Proprietary Name	Acyclovir
Dosage Form	CAPSULE
Usage	ORAL
Start Marketing Date	20241108
Marketing Category Name	ANDA
Application Number	ANDA204313
Manufacturer	Coupler LLC
Substance Name	ACYCLOVIR
Strength	200
Strength Unit	mg/1
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]