NDC11 63304011290
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 |
|---|---|
| 63304-0112-90 | 63304-0112 |
| 63304-112-90 | 63304-112 |
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 |
|---|---|---|---|---|---|---|
| droxidopa | DROXIDOPA | Sun Pharmaceutical Industries, Inc. | 51ef3096-4622-4f45-a180-ab0dc6d46df9 | 2021-02-18 | Boxed warning, Warnings, Adverse reactions | 63304-112-90 63304-112 63304011290 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.