"65691-0006-1" National Drug Code (NDC)

NDC Code	65691-0006-1
Package Description	100 TABLET in 1 BOTTLE (65691-0006-1)
Product NDC	65691-0006
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Acyclovir
Non-Proprietary Name	Acyclovir
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20120308
Marketing Category Name	ANDA
Application Number	ANDA202168
Manufacturer	Cadila Pharmaceuticals Limited
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 [Chemical/Ingredient]