NDC11 00527124202
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 |
|---|---|
| 00527-1242-02 | 00527-1242 |
| 00527-1242-2 | 00527-1242 |
| 0527-1242-02 | 0527-1242 |
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 |
|---|---|---|---|---|---|---|
| Fludarabine Phosphate | FLUDARABINE PHOSPHATE | Lannett Company, Inc. | 0170c0f4-d502-4f8f-bdbf-6439f3ed33fb | 2023-01-31 | Boxed warning, Warnings, Adverse reactions | 0527-1242-02 0527-1242 00527124202 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.