DHE 5.2 MG Nasal Powder [Atzumi]

RxCUI
2714192
RxNorm name
DHE 5.2 MG Nasal Powder [Atzumi]
Display name
DHE 5.2 MG Nasal Powder [Atzumi]
Full name
DHE 5.2 MG Nasal Powder [Atzumi]
Term type
SY
Status
DailyMed mapping
Updated
2026-06-04 23:38:46

RxNav Current And Historical NDCs#

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UNII Substances#

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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.

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Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
ATZUMIDIHYDROERGOTAMINE MESYLATESatsuma Pharmaceuticals, Inc.0982a44a-dc0c-75c0-e063-6394a90a6d6c2026-06-22Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 2714192

DailyMed RxNorm Mappings#

Set ID, RxNorm string, TTY table
Set IDRxNorm stringTTYSPL versionLabelEffective
0982a44a-dc0c-75c0-e063-6394a90a6d6cDHE 5.2 MG Nasal Powder [Atzumi]SY2These highlights do not include all the information needed to use ATZUMI safely and effectively. See full prescribing information for ATZUMI. ATZUMI™ (dihydroergotamine) nasal powder Initial U.S. Approval: 194620250508
0982a44a-dc0c-75c0-e063-6394a90a6d6cAtzumi 5.2 MG Nasal PowderSY2These highlights do not include all the information needed to use ATZUMI safely and effectively. See full prescribing information for ATZUMI. ATZUMI™ (dihydroergotamine) nasal powder Initial U.S. Approval: 194620250508
0982a44a-dc0c-75c0-e063-6394a90a6d6cdihydroergotamine 5.2 MG Nasal Powder [Atzumi]SBD2These highlights do not include all the information needed to use ATZUMI safely and effectively. See full prescribing information for ATZUMI. ATZUMI™ (dihydroergotamine) nasal powder Initial U.S. Approval: 194620250508
0982a44a-dc0c-75c0-e063-6394a90a6d6cAtzumi 5.2 MG Nasal PowderPSN2These highlights do not include all the information needed to use ATZUMI safely and effectively. See full prescribing information for ATZUMI. ATZUMI™ (dihydroergotamine) nasal powder Initial U.S. Approval: 194620250508