"0093-8943-01" National Drug Code (NDC)

NDC Code	0093-8943-01
Package Description	100 TABLET in 1 BOTTLE (0093-8943-01)
Product NDC	0093-8943
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Acyclovir
Non-Proprietary Name	Acyclovir
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	19970423
End Marketing Date	20200229
Marketing Category Name	ANDA
Application Number	ANDA074556
Manufacturer	Teva Pharmaceuticals USA, Inc.
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]