NDC11 71288013301
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 |
|---|---|
| 71288-0133-01 | 71288-0133 |
| 71288-0133-1 | 71288-0133 |
| 71288-133-01 | 71288-133 |
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 |
|---|---|---|---|---|---|---|
| Docetaxel | DOCETAXEL | Meitheal Pharmaceuticals Inc. | f970e352-3d43-4cc4-a859-503ec37b6e22 | 2025-05-15 | Boxed warning, Warnings, Adverse reactions | 71288-133-01 71288-133 71288013301 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.