NDC11 65862051730
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 |
|---|---|
| 65862-0517-30 | 65862-0517 |
| 65862-517-30 | 65862-517 |
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 |
|---|---|---|---|---|---|---|
| Risedronate Sodium | RISEDRONATE SODIUM | Aurobindo Pharma Limited | 89896dfe-f69d-4cb3-bb71-7a7c611071fa | 2026-02-11 | Warnings, Adverse reactions | 65862-517-30 65862-517 65862051730 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.