{
"NDC": {
"NDCCode": "62959-750-74",
"PackageDescription": "1 BOTTLE in 1 CARTON (62959-750-74) > 100 TABLET, FILM COATED in 1 BOTTLE",
"NDC11Code": "62959-0750-74",
"ProductNDC": "62959-750",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "Ibuprofen",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Ibuprofen 200mg",
"DosageFormName": "TABLET, FILM COATED",
"RouteName": "ORAL",
"StartMarketingDate": "20191212",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA209076",
"LabelerName": "ULTRAtab Laboratories, Inc.",
"SubstanceName": "IBUPROFEN",
"StrengthNumber": "200",
"StrengthUnit": "mg/1",
"Pharm_Classes": null,
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2020-10-06",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20211231",
"StartMarketingDatePackage": "20191212",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}