NDC11 50090677800
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 |
|---|---|
| 50090-6778-0 | 50090-6778 |
| 50090-6778-00 | 50090-6778 |
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 |
|---|---|---|---|---|---|---|
| Labetalol hydrochloride | LABETALOL HYDROCHLORIDE | A-S Medication Solutions | 83a6e770-207a-46bc-992d-c1ad90d1006d | 2023-10-30 | Warnings, Adverse reactions | 50090-6778-0 50090-6778 50090677800 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.