"71335-0708-0" National Drug Code (NDC)

Valacyclovir Hydrochloride 60 TABLET, FILM COATED in 1 BOTTLE (71335-0708-0)
(Bryant Ranch Prepack)

NDC Code71335-0708-0
Package Description60 TABLET, FILM COATED in 1 BOTTLE (71335-0708-0)
Product NDC71335-0708
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameValacyclovir Hydrochloride
Non-Proprietary NameValacyclovir Hydrochloride
Dosage FormTABLET, FILM COATED
UsageORAL
Start Marketing Date20100524
Marketing Category NameANDA
Application NumberANDA090682
ManufacturerBryant Ranch Prepack
Substance NameVALACYCLOVIR HYDROCHLORIDE
Strength500
Strength Unitmg/1
Pharmacy ClassesDNA 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]

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