FDA.reportPublic FDA data

Ojemda 600 MG Weekly Dose Carton Pack, 4 Blister Cards, 6 Tablets Each

RxCUI
2690862
RxNorm name
Ojemda 600 MG Weekly Dose Carton Pack, 4 Blister Cards, 6 Tablets Each
Display name
Ojemda 600 MG Weekly Dose Carton Pack, 4 Blister Cards, 6 Tablets Each
Full name
Ojemda 600 MG Weekly Dose Carton Pack, 4 Blister Cards, 6 Tablets Each
Term type
SY
Status
DailyMed mapping
Updated
2026-06-04 23:39:26

RxNav Current And Historical NDCs#

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UNII Substances#

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openFDA label cross-check#

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

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
OJEMDATOVORAFENIBDay One Biopharmaceuticals, Inc.ea3a9631-3a66-6a7c-e053-2995a90ae2ad2025-09-02Warnings, Adverse reactionsExact identifier
rxcui: 2690862

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
ea3a9631-3a66-6a7c-e053-2995a90ae2ad{24 (tovorafenib 100 MG Oral Tablet [Ojemda]) } Pack [Ojemda 600 MG Once Weekly Carton] [BPCK] · ojemda 600 MG Weekly Dose Carton Pack [PSN] · Ojemda 600 MG Weekly Dose Carton Pack, 4 Blister Cards, 6 Tablets Each [SY]39These highlights do not include all the information needed to use OJEMDA safely and effectively. See full prescribing information for OJEMDA. OJEMDA (tovorafenib) tablets, for oral use OJEMDA (tovorafenib) for oral suspension Initial U.S. Approval: 202420250902