NDC11 67877070505
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 |
|---|---|
| 67877-0705-05 | 67877-0705 |
| 67877-0705-5 | 67877-0705 |
| 67877-705-05 | 67877-705 |
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 | Ascend Laboratories, LLC | 6091958e-f04e-47c0-9eef-9c204df4edd9 | 2025-07-21 | Boxed warning, Warnings, Adverse reactions | 67877-705-05 67877-705 67877070505 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.