{90 (lenvatinib 4 MG Oral Capsule [Lenvima]) } Pack [Lenvima 12]
- RxCUI
- 2054159
- RxNorm name
- {90 (lenvatinib 4 MG Oral Capsule [Lenvima]) } Pack [Lenvima 12]
- Display name
- {90 (lenvatinib 4 MG Oral Capsule [Lenvima]) } Pack [Lenvima 12]
- Full name
- {90 (lenvatinib 4 MG Oral Capsule [Lenvima]) } Pack [Lenvima 12]
- Term type
- BPCK
- Status
- DailyMed mapping
- Updated
- 2026-06-04 23:39:28
UNII Substances#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Lenvima | LENVATINIB | Eisai Inc. | f4bedd21-efde-44c6-9d9c-b48b78d7ed1e | 2026-06-30 | Warnings, Adverse reactions | 2054159 |
DailyMed RxNorm Mappings#
| Set ID | RxNorm string | TTY | SPL version | Label | Effective |
|---|---|---|---|---|---|
| f4bedd21-efde-44c6-9d9c-b48b78d7ed1e | {90 (lenvatinib 4 MG Oral Capsule [Lenvima]) } Pack [Lenvima 12] | BPCK | 78 | These highlights do not include all the information needed to use LENVIMA safely and effectively. See full prescribing information for LENVIMA . LENVIMA ® ( lenvatinib ) capsules , for oral use Initial U.S. Approval: 2015 | 20250103 |
| f4bedd21-efde-44c6-9d9c-b48b78d7ed1e | Lenvima 12 MG daily dose 30 Day Supply Pack | PSN | 78 | These highlights do not include all the information needed to use LENVIMA safely and effectively. See full prescribing information for LENVIMA . LENVIMA ® ( lenvatinib ) capsules , for oral use Initial U.S. Approval: 2015 | 20250103 |
| f4bedd21-efde-44c6-9d9c-b48b78d7ed1e | Lenvima 12 MG (as lenvatinib mesylate) Daily Dose 30 Day Supply Pack | SY | 78 | These highlights do not include all the information needed to use LENVIMA safely and effectively. See full prescribing information for LENVIMA . LENVIMA ® ( lenvatinib ) capsules , for oral use Initial U.S. Approval: 2015 | 20250103 |