NDC11 71258002201
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 |
|---|---|
| 71258-0022-01 | 71258-0022 |
| 71258-0022-1 | 71258-0022 |
| 71258-022-01 | 71258-022 |
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 |
|---|---|---|---|---|---|---|
| PYLARIFY | PIFLUFOLASTAT F-18 | Progenics Pharmaceuticals, Inc. | a00e5cbc-4fd5-4280-82ec-cd3498df4553 | 2026-02-18 | Warnings, Adverse reactions | 71258-022-01 71258-022 71258002201 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.