{
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"PackageDescription": "1 BOTTLE in 1 CARTON (72579-022-08) / 120 TABLET, FILM COATED in 1 BOTTLE",
"NDC11Code": "72579-0022-08",
"ProductNDC": "72579-022",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Beqalzi",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Sonrotoclax",
"DosageFormName": "TABLET, FILM COATED",
"RouteName": "ORAL",
"StartMarketingDate": "20260831",
"EndMarketingDate": null,
"MarketingCategoryName": "NDA",
"ApplicationNumber": "NDA220711",
"LabelerName": "BeOne Medicines USA, Inc.",
"SubstanceName": "SONROTOCLAX",
"StrengthNumber": "80",
"StrengthUnit": "mg/1",
"Pharm_Classes": null,
"DEASchedule": null,
"Status": "Active",
"LastUpdate": "2026-08-31",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20271231",
"StartMarketingDatePackage": "20260831",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}