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
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 |
|---|---|---|---|---|---|---|
| PROMACTA | ELTROMBOPAG OLAMINE | Novartis Pharmaceuticals Corporation | 7714a0ed-34bb-46e6-a0a5-b363908b22c2 | 2025-12-18 | Boxed warning, Warnings, Adverse reactions | 1859501 |
DailyMed RxNorm Mappings#
| Set ID | RxNorm mappings | Terms | SPL version | Label | Effective |
|---|---|---|---|---|---|
| 7714a0ed-34bb-46e6-a0a5-b363908b22c2 | Promacta 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] | 4 | 31 | These 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: 2008 | 20251218 |