NDC11 71394071601
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 |
|---|---|
| 71394-0716-01 | 71394-0716 |
| 71394-0716-1 | 71394-0716 |
| 71394-716-01 | 71394-716 |
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 |
|---|---|---|---|---|---|---|
| LUXTURNA | VORETIGENE NEPARVOVEC-RZYL | Spark Therapeutics, Inc. | 08313a24-e7ce-457a-bb3f-161bc45517ee | 2022-05-01 | Warnings, Adverse reactions | 71394-716-01 71394071601 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.