{
"NDC": {
"NDCCode": "68071-4611-4",
"PackageDescription": "118 mL in 1 BOTTLE (68071-4611-4) ",
"NDC11Code": "68071-4611-04",
"ProductNDC": "68071-4611",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "Ibuprofen",
"ProprietaryNameSuffix": "Childrens",
"NonProprietaryName": "Ibuprofen",
"DosageFormName": "SUSPENSION",
"RouteName": "ORAL",
"StartMarketingDate": "20180112",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA074916",
"LabelerName": "NuCare Pharmaceuticals,Inc.",
"SubstanceName": "IBUPROFEN",
"StrengthNumber": "100",
"StrengthUnit": "mg/5mL",
"Pharm_Classes": null,
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2020-06-17",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20201231",
"StartMarketingDatePackage": "20181022",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}