FDA.reportPublic FDA data

donepezil hydrochloride 10 MG Disintegrating Oral Tablet [Aricept]

RxCUI
997222
RxNorm name
donepezil hydrochloride 10 MG Disintegrating Oral Tablet [Aricept]
Display name
donepezil hydrochloride 10 MG Disintegrating Oral Tablet [Aricept]
Full name
donepezil hydrochloride 10 MG Disintegrating Oral Tablet [Aricept]
Term type
SBD
Status
DailyMed mapping
Updated
2026-06-04 23:39:09

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.

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

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
AriceptDONEPEZIL HYDROCHLORIDEEisai Inc.98e451e1-e4d7-4439-a675-c5457ba209752021-12-30Warnings, Adverse reactionsExact identifier
rxcui: 997222

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
98e451e1-e4d7-4439-a675-c5457ba20975Aricept ODT 10 MG Disintegrating Oral Tablet [PSN] · donepezil hydrochloride 10 MG Disintegrating Oral Tablet [Aricept] [SBD] · Aricept 10 MG Disintegrating Oral Tablet [SY] · Aricept ODT 10 MG Disintegrating Oral Tablet [SY]431These highlights do not include all the information needed to use ARICEPT safely and effectively. See full prescribing information for ARICEPT. ARICEPT ® (donepezil hydrochloride) tablets, for oral use ARICEPT ODT (donepezil hydrochloride) orally disintegrating tablets Initial U.S. Approval: 199620211201