{
"NDC": {
"NDCCode": "68071-4353-6",
"PackageDescription": "60 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-4353-6) ",
"NDC11Code": "68071-4353-06",
"ProductNDC": "68071-4353",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Rabeprazole Sodium",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Rabeprazole Sodium",
"DosageFormName": "TABLET, DELAYED RELEASE",
"RouteName": "ORAL",
"StartMarketingDate": "20170601",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA204237",
"LabelerName": "NuCare Pharmaceuticals,Inc.",
"SubstanceName": "RABEPRAZOLE SODIUM",
"StrengthNumber": "20",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2020-01-01",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20191231",
"StartMarketingDatePackage": "20180323",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}