NDC11 16714052820
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 |
|---|---|
| 16714-0528-20 | 16714-0528 |
| 16714-528-20 | 16714-528 |
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 |
|---|---|---|---|---|---|---|
| propofol | PROPOFOL | NorthStar Rx LLC | 5ec25932-6c21-4cd5-8f60-80761f2e20a6 | 2025-05-26 | Warnings, Adverse reactions | 16714-528-20 16714-528 16714052820 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.