{
"NDC": {
"NDCCode": "68071-4587-2",
"PackageDescription": "200 mL in 1 BOTTLE (68071-4587-2) ",
"NDC11Code": "68071-4587-02",
"ProductNDC": "68071-4587",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Cephalexin",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Cephalexin",
"DosageFormName": "POWDER, FOR SUSPENSION",
"RouteName": "ORAL",
"StartMarketingDate": "19900930",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA062703",
"LabelerName": "NuCare Pharmaceuticals,Inc.",
"SubstanceName": "CEPHALEXIN",
"StrengthNumber": "125",
"StrengthUnit": "mg/5mL",
"Pharm_Classes": "Cephalosporin Antibacterial [EPC],Cephalosporins [CS]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2020-06-17",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20201231",
"StartMarketingDatePackage": "20181005",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}