{
"NDC": {
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"PackageDescription": "100 TABLET in 1 BOTTLE (81469-221-01) ",
"NDC11Code": "81469-0221-01",
"ProductNDC": "81469-221",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Bumetanide",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Bumetanide",
"DosageFormName": "TABLET",
"RouteName": "ORAL",
"StartMarketingDate": "20260219",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA219291",
"LabelerName": "First Nation Group, LLC",
"SubstanceName": "BUMETANIDE",
"StrengthNumber": ".5",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Increased Diuresis at Loop of Henle [PE], Loop Diuretic [EPC]",
"DEASchedule": null,
"Status": "Active",
"LastUpdate": "2026-02-20",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20271231",
"StartMarketingDatePackage": "20260219",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}