NDC11 55150019183
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 |
|---|---|
| 55150-0191-83 | 55150-0191 |
| 55150-191-83 | 55150-191 |
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 |
|---|---|---|---|---|---|---|
| Ibandronate Sodium | IBANDRONATE SODIUM | Eugia US LLC | e81f2c5b-bead-48ac-be3e-016cf963d7ed | 2026-01-27 | Warnings, Adverse reactions | 55150-191-83 55150-191 55150019183 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.