deflazacort 6 MG Oral Tablet [Emflaza]

RxCUI
1870950
RxNorm name
deflazacort 6 MG Oral Tablet [Emflaza]
Display name
deflazacort 6 MG Oral Tablet [Emflaza]
Full name
deflazacort 6 MG Oral Tablet [Emflaza]
Term type
SBD
Status
DailyMed mapping
Updated
2026-06-04 23:38:52

RxNav Current And Historical NDCs#

RxNav current and historical NDC rows page 1 of 1 · 0 matching rows.

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: 1870950

DailyMed RxNorm Mappings#

Set ID, RxNorm string, TTY table
Set IDRxNorm stringTTYSPL versionLabelEffective
31b347d2-f156-4055-9d8f-7cf0df420296deflazacort 6 MG Oral Tablet [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 6 MG Oral TabletPSN21These 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 6 MG Oral TabletSY21These 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