NDC11 65219042950
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 |
|---|---|
| 65219-0429-50 | 65219-0429 |
| 65219-429-50 | 65219-429 |
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 |
|---|---|---|---|---|---|---|
| Argatroban | ARGATROBAN | Fresenius Kabi USA, LLC | dfa5d325-f609-4c9a-aaae-1a17df47da1e | 2025-09-03 | Warnings, Adverse reactions | 65219-429-50 65219-429 65219042950 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.