NDC11 43598050530
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 |
|---|---|
| 43598-0505-30 | 43598-0505 |
| 43598-505-30 | 43598-505 |
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 | Dr.Reddys Laboratories Inc | 8f24455c-34dc-4e07-bcd3-24326b9cc377 | 2022-12-23 | Boxed warning, Warnings, Adverse reactions | 43598-505-30 43598-505 43598050530 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.