eslicarbazepine acetate 800 MG Oral Tablet [Aptiom]

RxCUI
1482527
RxNorm name
eslicarbazepine acetate 800 MG Oral Tablet [Aptiom]
Display name
eslicarbazepine acetate 800 MG Oral Tablet [Aptiom]
Full name
eslicarbazepine acetate 800 MG Oral Tablet [Aptiom]
Term type
SBD
Status
DailyMed mapping
Updated
2026-06-04 23:38:54

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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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
AptiomESLICARBAZEPINE ACETATESumitomo Pharma America, Inc.3d0c9554-eaeb-4694-8089-00133fcadce32023-11-10Warnings, Adverse reactionsExact identifier
rxcui: 1482527

DailyMed RxNorm Mappings#

Set ID, RxNorm string, TTY table
Set IDRxNorm stringTTYSPL versionLabelEffective
3d0c9554-eaeb-4694-8089-00133fcadce3eslicarbazepine acetate 800 MG Oral Tablet [Aptiom]SBD16These highlights do not include all the information needed to use APTIOM safely and effectively. See full prescribing information for APTIOM. APTIOM ® (eslicarbazepine acetate) tablets, for oral use Initial U.S. Approval: 201320231110
3d0c9554-eaeb-4694-8089-00133fcadce3Aptiom 800 MG Oral Tablet, Once DailyPSN16These highlights do not include all the information needed to use APTIOM safely and effectively. See full prescribing information for APTIOM. APTIOM ® (eslicarbazepine acetate) tablets, for oral use Initial U.S. Approval: 201320231110
3d0c9554-eaeb-4694-8089-00133fcadce3Aptiom 800 MG Oral TabletSY16These highlights do not include all the information needed to use APTIOM safely and effectively. See full prescribing information for APTIOM. APTIOM ® (eslicarbazepine acetate) tablets, for oral use Initial U.S. Approval: 201320231110