NDC11 50090146700
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 |
|---|---|
| 50090-1467-0 | 50090-1467 |
| 50090-1467-00 | 50090-1467 |
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 |
|---|---|---|---|---|---|---|
| Budesonide | BUDESONIDE | A-S Medication Solutions | 32e30f11-e19b-4e23-a893-92d95e48edef | 2023-11-29 | Warnings, Adverse reactions | 50090-1467-0 50090-1467 50090146700 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.