"61786-088-02" National Drug Code (NDC)

NDC Code	61786-088-02
Package Description	30 CAPSULE in 1 BLISTER PACK (61786-088-02)
Product NDC	61786-088
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Zovirax
Non-Proprietary Name	Acyclovir
Dosage Form	CAPSULE
Usage	ORAL
Start Marketing Date	20141110
Marketing Category Name	NDA
Application Number	NDA018828
Manufacturer	REMEDYREPACK INC.
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 [Chemical/Ingredient]