{
"NDC": {
"NDCCode": "42291-277-30",
"PackageDescription": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (42291-277-30) ",
"NDC11Code": "42291-0277-30",
"ProductNDC": "42291-277",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Famciclovir",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Famciclovir",
"DosageFormName": "TABLET, FILM COATED",
"RouteName": "ORAL",
"StartMarketingDate": "20120104",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA077487",
"LabelerName": "AvKARE, Inc.",
"SubstanceName": "FAMCICLOVIR",
"StrengthNumber": "500",
"StrengthUnit": "mg/1",
"Pharm_Classes": "DNA Polymerase Inhibitors [MoA],Herpesvirus Nucleoside Analog DNA Polymerase Inhibitor [EPC],Nucleoside Analog [EXT]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2020-06-17",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20211231",
"StartMarketingDatePackage": "20120104",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}