FDA.reportPublic FDA data

Otezla 14-Day 10/20 Starter Pack

RxCUI
2682432
RxNorm name
Otezla 14-Day 10/20 Starter Pack
Display name
Otezla 14-Day 10/20 Starter Pack
Full name
Otezla 14-Day 10/20 Starter Pack
Term type
SY
Status
DailyMed mapping
Updated
2026-06-04 23:39:28

RxNav Current And Historical NDCs#

RxNav current and historical NDC rows page 1 of 1 · 0 matching rows.

No records found.

UNII Substances#

UNII substance links page 1 of 1 · 0 matching rows.

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
OtezlaAPREMILASTAmgen, Incf6b1f516-4972-4d82-bced-113e47b41cc52025-12-23Warnings, Adverse reactionsExact identifier
rxcui: 2682432

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
f6b1f516-4972-4d82-bced-113e47b41cc5{4 (apremilast 10 MG Oral Tablet [Otezla]) / 23 (apremilast 20 MG Oral Tablet [Otezla]) } Pack [Otezla 14-Day 10/20 Starter Pack] [BPCK] · Otezla 14-Day 10/20 Starter Pack [PSN] · Otezla 14-Day 10/20 Starter Pack [SY]334These highlights do not include all the information needed to use OTEZLA/OTEZLA XR safely and effectively. See full prescribing information for OTEZLA/OTEZLA XR. OTEZLA ® (apremilast) tablets, for oral use OTEZLA XR™ (apremilast) extended-release tablets, for oral use Initial U.S. Approval: 201420251223