NDC11 55150038601
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 |
|---|---|
| 55150-0386-01 | 55150-0386 |
| 55150-0386-1 | 55150-0386 |
| 55150-386-01 | 55150-386 |
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 |
|---|---|---|---|---|---|---|
| CARBOPLATIN | CARBOPLATIN | Eugia US LLC | 5abfcb87-bb02-4384-9c9d-7d0e3e809311 | 2025-01-30 | Boxed warning, Warnings, Adverse reactions | 55150-386 |
| CARBOPLATIN | CARBOPLATIN | Eugia US LLC | f5fe9a20-47a5-45b9-ab06-c6158d9b6aca | 2025-01-10 | Boxed warning, Warnings, Adverse reactions | 55150-386-01 55150-386 55150038601 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.