"71335-0695-3" National Drug Code (NDC)

Acyclovir 30 TABLET in 1 BOTTLE (71335-0695-3)
(Bryant Ranch Prepack)

NDC Code71335-0695-3
Package Description30 TABLET in 1 BOTTLE (71335-0695-3)
Product NDC71335-0695
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NameAcyclovir
Non-Proprietary NameAcyclovir
Dosage FormTABLET
UsageORAL
Start Marketing Date20131129
Marketing Category NameANDA
Application NumberANDA203834
ManufacturerBryant Ranch Prepack
Substance NameACYCLOVIR
Strength800
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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