<?xml version="1.0" encoding="UTF-8"?>
<NDC>
<NDCCode>
72579-999-99
</NDCCode>
<PackageDescription>
24 BOTTLE, PLASTIC in 1 PACKAGE (72579-999-99) / 120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
</PackageDescription>
<NDC11Code>
72579-0999-99
</NDC11Code>
<ProductNDC>
72579-999
</ProductNDC>
<ProductTypeName>
DRUG FOR FURTHER PROCESSING
</ProductTypeName>
<ProprietaryName/>
<ProprietaryNameSuffix/>
<NonProprietaryName>
Sonrotoclax
</NonProprietaryName>
<DosageFormName>
TABLET, FILM COATED
</DosageFormName>
<RouteName/>
<StartMarketingDate>
20260911
</StartMarketingDate>
<EndMarketingDate/>
<MarketingCategoryName>
DRUG FOR FURTHER PROCESSING
</MarketingCategoryName>
<ApplicationNumber/>
<LabelerName>
BeOne Medicines USA, Inc.
</LabelerName>
<SubstanceName>
SONROTOCLAX
</SubstanceName>
<StrengthNumber>
80
</StrengthNumber>
<StrengthUnit>
mg/1
</StrengthUnit>
<Pharm_Classes/>
<DEASchedule/>
<Status>
Unfinished
</Status>
<LastUpdate>
2026-09-16
</LastUpdate>
<PackageNdcExcludeFlag/>
<ProductNdcExcludeFlag/>
<ListingRecordCertifiedThrough>
20271231
</ListingRecordCertifiedThrough>
<StartMarketingDatePackage>
11-SEP-26
</StartMarketingDatePackage>
<EndMarketingDatePackage/>
<SamplePackage/>
</NDC>