NDC11 00135057601
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 |
|---|---|
| 00135-0576-01 | 00135-0576 |
| 00135-0576-1 | 00135-0576 |
| 00135-576-01 | 00135-576 |
| 0135-0576-01 | 0135-0576 |
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 |
|---|---|---|---|---|---|---|
| FLONASE ALLERGY RELIEF | FLUTICASONE PROPIONATE | Haleon US Holdings LLC | b6134ba0-b70a-4eac-9a82-cef64b242c1d | 2024-12-19 | Warnings | 0135-0576-01 0135-0576 00135057601 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.