{
"NDC": {
"NDCCode": "0832-6080-03",
"PackageDescription": "30 TABLET in 1 BOTTLE (0832-6080-03) ",
"NDC11Code": "00832-6080-03",
"ProductNDC": "0832-6080",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Olanzapine",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Olanzapine",
"DosageFormName": "TABLET",
"RouteName": "ORAL",
"StartMarketingDate": "20160127",
"EndMarketingDate": "20260831",
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA204319",
"LabelerName": "Upsher-Smith Laboratories, LLC",
"SubstanceName": "OLANZAPINE",
"StrengthNumber": "7.5",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Atypical Antipsychotic [EPC]",
"DEASchedule": null,
"Status": "Active",
"LastUpdate": "2025-11-28",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": null,
"StartMarketingDatePackage": "20240815",
"EndMarketingDatePackage": "20260831",
"SamplePackage": "N"
}
}