FDA.reportPublic FDA data

Zunveyl 5 MG Delayed Release Oral Tablet

RxCUI
2690638
RxNorm name
Zunveyl 5 MG Delayed Release Oral Tablet
Display name
Zunveyl 5 MG Delayed Release Oral Tablet
Full name
Zunveyl 5 MG Delayed Release Oral Tablet
Term type
SY
Status
DailyMed mapping
Updated
2026-06-04 23:39:16

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
ZUNVEYLBENZGALANTAMINEAlpha Cognition, Inc.af47bf67-1f07-4650-8064-24c38afc46562026-03-17Warnings, Adverse reactionsExact identifier
rxcui: 2690638

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

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
af47bf67-1f07-4650-8064-24c38afc4656ZUNVEYL 5 MG Delayed Release Oral Tablet [PSN] · benzgalantamine 5 MG Delayed Release Oral Tablet [Zunveyl] [SBD] · Zunveyl 5 MG Delayed Release Oral Tablet [SY]35These highlights do not include all the information needed to use ZUNVEYL safely and effectively. See full prescribing information for ZUNVEYL. ZUNVEYL (benzgalantamine) delayed-release tablets, for oral use Initial U.S. Approval: 200120260317