"49349-620-02" National Drug Code (NDC)

NDC Code	49349-620-02
Package Description	30 CAPSULE in 1 BLISTER PACK (49349-620-02)
Product NDC	49349-620
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Acyclovir
Non-Proprietary Name	Acyclovir
Dosage Form	CAPSULE
Usage	ORAL
Start Marketing Date	20111206
Marketing Category Name	ANDA
Application Number	ANDA074578
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]