NDC11 69794000101
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 |
|---|---|
| 69794-0001-01 | 69794-0001 |
| 69794-0001-1 | 69794-0001 |
| 69794-001-01 | 69794-001 |
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 |
|---|---|---|---|---|---|---|
| MEPSEVII | VESTRONIDASE ALFA | Ultragenyx Pharmaceutical Inc. | 925d4e21-fd98-474d-a34d-a0b3558ed750 | 2025-11-18 | Boxed warning, Warnings, Adverse reactions | 69794-001-01 69794-001 69794000101 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.