FDA.reportPublic FDA data

100 ML albumin human, USP 250 MG/ML Injection [Flexbumin]

RxCUI
1742403
RxNorm name
100 ML albumin human, USP 250 MG/ML Injection [Flexbumin]
Display name
100 ML albumin human, USP 250 MG/ML Injection [Flexbumin]
Full name
100 ML albumin human, USP 250 MG/ML Injection [Flexbumin]
Term type
SBD
Status
DailyMed mapping
Updated
2026-06-04 23:39:19

Purple Book Biologic Products#

BLA, Proprietary name, Proper name table
BLAProprietary nameProper nameLicense typeStatusLatest source
101452Buminate, FlexbuminAlbumin (Human)351(a)Rx2026-06-01

RxNav Current And Historical NDCs#

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UNII Substances#

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DailyMed RxNorm Mappings#

Set ID, RxNorm string, TTY table
Set IDRxNorm stringTTYSPL versionLabelEffective
bdb4e167-27a2-4b50-b245-43df9cd535cb100 ML albumin human, USP 250 MG/ML Injection [Flexbumin]SBD17These highlights do not include all the information needed to use FLEXBUMIN ® 25% safely and effectively. See full prescribing information for FLEXBUMIN 25%. FLEXBUMIN ® 25% Albumin (Human), USP, 25% Solution, for intravenous use Initial U.S. Approval: 200520241218
bdb4e167-27a2-4b50-b245-43df9cd535cbFlexbumin 25 GM per 100 ML InjectionSY17These highlights do not include all the information needed to use FLEXBUMIN ® 25% safely and effectively. See full prescribing information for FLEXBUMIN 25%. FLEXBUMIN ® 25% Albumin (Human), USP, 25% Solution, for intravenous use Initial U.S. Approval: 200520241218
bdb4e167-27a2-4b50-b245-43df9cd535cbFlexbumin 25 % per 100 ML InjectionSY17These highlights do not include all the information needed to use FLEXBUMIN ® 25% safely and effectively. See full prescribing information for FLEXBUMIN 25%. FLEXBUMIN ® 25% Albumin (Human), USP, 25% Solution, for intravenous use Initial U.S. Approval: 200520241218
bdb4e167-27a2-4b50-b245-43df9cd535cbFLEXBUMIN 25 % in 100 ML InjectionPSN17These highlights do not include all the information needed to use FLEXBUMIN ® 25% safely and effectively. See full prescribing information for FLEXBUMIN 25%. FLEXBUMIN ® 25% Albumin (Human), USP, 25% Solution, for intravenous use Initial U.S. Approval: 200520241218