"10544-027-25" National Drug Code (NDC)

NDC Code	10544-027-25
Package Description	25 TABLET in 1 BOTTLE, PLASTIC (10544-027-25)
Product NDC	10544-027
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Acyclovir
Non-Proprietary Name	Acyclovir
Dosage Form	TABLET
Usage	ORAL
Start Marketing Date	20101110
End Marketing Date	20170831
Marketing Category Name	ANDA
Application Number	ANDA075382
Manufacturer	Blenheim Pharmacal, Inc.
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 [Chemical/Ingredient]