Promacta 25 MG Powder for Oral Suspension

RxCUI
1859501
RxNorm name
Promacta 25 MG Powder for Oral Suspension
Display name
Promacta 25 MG Powder for Oral Suspension
Full name
Promacta 25 MG Powder for Oral Suspension
Term type
PSN
Status
DailyMed mapping
Updated
2026-06-04 23:39:04

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.

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Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
PROMACTAELTROMBOPAG OLAMINENovartis Pharmaceuticals Corporation7714a0ed-34bb-46e6-a0a5-b363908b22c22025-12-18Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 1859501

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
7714a0ed-34bb-46e6-a0a5-b363908b22c2Promacta 25 MG Powder for Oral Suspension [PSN] · eltrombopag 25 MG Powder for Oral Suspension [Promacta] [SBD] · Promacta 25 MG Powder for Oral Suspension [SY] · Promacta eltrombopag 25 MG (as eltrombopag olamine) Powder for Oral Suspension [SY]431These highlights do not include all the information needed to use PROMACTA safely and effectively. See full prescribing information for PROMACTA. PROMACTA ® (eltrombopag) tablets, for oral use PROMACTA ® (eltrombopag) for oral suspension Initial U.S. Approval: 200820251218