NDC11 00074445651
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 |
|---|---|
| 00074-4456-51 | 00074-4456 |
| 0074-4456-51 | 0074-4456 |
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 |
|---|---|---|---|---|---|---|
| Ultane | SEVOFLURANE | AbbVie Inc. | c9aa6489-5a36-44ed-9512-b996833d82f7 | 2025-02-12 | Warnings, Adverse reactions | 0074-4456-51 0074-4456 00074445651 |
| Ultane | SEVOFLURANE | AbbVie Inc. | 4c6e76bc-c964-4955-e0a3-511d3386a9cc | 2025-01-13 | Warnings, Adverse reactions | 0074-4456 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.