NDC11 55150028399
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 |
|---|---|
| 55150-0283-99 | 55150-0283 |
| 55150-283-99 | 55150-283 |
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 |
|---|---|---|---|---|---|---|
| Zoledronic Acid | ZOLEDRONIC ACID | Eugia US LLC | bf5f96d4-f87c-4968-bed0-a4b5e77f4162 | 2026-05-15 | Warnings, Adverse reactions | 55150-283-99 55150-283 55150028399 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.