FDA.reportPublic FDA data

divalproex sodium 250 MG Delayed Release Oral Tablet [Depakote]

RxCUI
1099679
RxNorm name
divalproex sodium 250 MG Delayed Release Oral Tablet [Depakote]
Display name
divalproex sodium 250 MG Delayed Release Oral Tablet [Depakote]
Full name
divalproex sodium 250 MG Delayed Release Oral Tablet [Depakote]
Term type
SBD
Status
DailyMed mapping
Updated
2026-06-04 23:38:46

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.

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Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
DepakoteDIVALPROEX SODIUMAbbVie Inc.08a65cf4-7749-4ceb-6895-8f4805e2b01f2026-03-31Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 1099679

DailyMed RxNorm Mappings#

unique DailyMed labels mapped to this RxNorm concept page 1 of 1 · 1 matching rows.

Set ID, RxNorm mappings, Terms table
Set IDRxNorm mappingsTermsSPL versionLabelEffective
08a65cf4-7749-4ceb-6895-8f4805e2b01fDepakote 250 MG Delayed Release Oral Tablet [PSN] · divalproex sodium 250 MG Delayed Release Oral Tablet [Depakote] [SBD] · Depakote 250 MG Delayed Release Oral Tablet [SY]31621These highlights do not include all the information needed to use Depakote safely and effectively. See full prescribing information for Depakote. Depakote (divalproex sodium) delayed-release tablets, for oral use Initial U.S. Approval: 198320260331