{
"NDC": {
"NDCCode": "30142-167-05",
"PackageDescription": "500 TABLET in 1 BOTTLE (30142-167-05) ",
"NDC11Code": "30142-0167-05",
"ProductNDC": "30142-167",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "Ibuprofen",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Ibuprofen",
"DosageFormName": "TABLET",
"RouteName": "ORAL",
"StartMarketingDate": "20110202",
"EndMarketingDate": "20190331",
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA072199",
"LabelerName": "The Kroger Co.",
"SubstanceName": "IBUPROFEN",
"StrengthNumber": "200",
"StrengthUnit": "mg/1",
"Pharm_Classes": null,
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2019-04-02",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": null,
"StartMarketingDatePackage": "20110202",
"EndMarketingDatePackage": "20190331",
"SamplePackage": "N"
}
}