NDC11 72241001022
This exact 11-digit normalized identifier can correspond to more than one FDA hyphenation. FDA.report preserves the exact identifier and exposes every structurally valid candidate without guessing.
Possible FDA NDC forms#
| Package NDC | Product root |
|---|---|
| 72241-0010-22 | 72241-0010 |
| 72241-010-22 | 72241-010 |
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 |
|---|---|---|---|---|---|---|
| Raloxifene hydrochloride | RALOXIFENE HYDROCHLORIDE | Modavar Pharmaceuticals LLC | f0db29f5-28da-4165-94f8-24727b6b71e5 | 2022-01-17 | Boxed warning, Warnings, Adverse reactions | 72241-010-22 72241-010 72241001022 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.