"67046-335-30" National Drug Code (NDC)

NDC Code	67046-335-30
Package Description	30 TABLET in 1 BLISTER PACK (67046-335-30)
Product NDC	67046-335
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Acyclovir
Non-Proprietary Name	Acyclovir
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20200615
Marketing Category Name	ANDA
Application Number	ANDA203834
Manufacturer	Contract Pharmacy Services-PA
Substance Name	ACYCLOVIR
Strength	400
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]