"70934-697-35" National Drug Code (NDC)

NDC Code	70934-697-35
Package Description	35 TABLET in 1 BOTTLE, PLASTIC (70934-697-35)
Product NDC	70934-697
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Acyclovir
Non-Proprietary Name	Acyclovir
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20200508
Marketing Category Name	ANDA
Application Number	ANDA077309
Manufacturer	Apotex Corp.
Substance Name	ACYCLOVIR
Strength	800
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]