NDC11 69452025719
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 |
|---|---|
| 69452-0257-19 | 69452-0257 |
| 69452-257-19 | 69452-257 |
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 | Bionpharma Inc. | c3cfd280-3548-b590-e053-2a95a90a5eb3 | 2021-06-02 | Boxed warning, Warnings, Adverse reactions | 69452-257-19 69452-257 69452025719 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.