deflazacort 22.75 MG/ML Oral Suspension [Emflaza]

RxCUI
1870968
RxNorm name
deflazacort 22.75 MG/ML Oral Suspension [Emflaza]
Display name
deflazacort 22.75 MG/ML Oral Suspension [Emflaza]
Full name
deflazacort 22.75 MG/ML Oral Suspension [Emflaza]
Term type
SBD
Status
DailyMed mapping
Updated
2026-06-04 23:38:52

RxNav Current And Historical NDCs#

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No records found.

UNII Substances#

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No records found.

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
EMFLAZADEFLAZACORTPTC Therapeutics, Inc.31b347d2-f156-4055-9d8f-7cf0df4202962025-11-13Warnings, Adverse reactionsExact identifier
rxcui: 1870968

DailyMed RxNorm Mappings#

Set ID, RxNorm string, TTY table
Set IDRxNorm stringTTYSPL versionLabelEffective
31b347d2-f156-4055-9d8f-7cf0df420296deflazacort 22.75 MG/ML Oral Suspension [Emflaza]SBD21These highlights do not include all the information needed to use EMFLAZA ® safely and effectively. See full prescribing information for EMFLAZA. EMFLAZA ® (deflazacort) tablets, for oral use EMFLAZA ® (deflazacort) oral suspension Initial U.S. Approval: 201720251113
31b347d2-f156-4055-9d8f-7cf0df420296Emflaza 22.75 MG/mL Oral SuspensionPSN21These highlights do not include all the information needed to use EMFLAZA ® safely and effectively. See full prescribing information for EMFLAZA. EMFLAZA ® (deflazacort) tablets, for oral use EMFLAZA ® (deflazacort) oral suspension Initial U.S. Approval: 201720251113
31b347d2-f156-4055-9d8f-7cf0df420296Emflaza 22.75 MG/ML Oral SuspensionSY21These highlights do not include all the information needed to use EMFLAZA ® safely and effectively. See full prescribing information for EMFLAZA. EMFLAZA ® (deflazacort) tablets, for oral use EMFLAZA ® (deflazacort) oral suspension Initial U.S. Approval: 201720251113