NDC11 16714082901
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 |
|---|---|
| 16714-0829-01 | 16714-0829 |
| 16714-0829-1 | 16714-0829 |
| 16714-829-01 | 16714-829 |
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 | Northstar Rx LLC. | a37866df-df07-4f71-8591-98c2804c4794 | 2025-02-18 | Warnings, Adverse reactions | 16714-829-01 16714-829 16714082901 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.