"53808-0628-2" National Drug Code (NDC)

NDC Code	53808-0628-2
Package Description	60 TABLET in 1 BLISTER PACK (53808-0628-2)
Product NDC	53808-0628
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Acyclovir
Non-Proprietary Name	Acyclovir
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20130101
Marketing Category Name	ANDA
Application Number	ANDA075382
Manufacturer	State of Florida DOH Central Pharmacy
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]