NDC11 71335084209
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 |
|---|---|
| 71335-0842-09 | 71335-0842 |
| 71335-0842-9 | 71335-0842 |
| 71335-842-09 | 71335-842 |
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 |
|---|---|---|---|---|---|---|
| Furosemide | FUROSEMIDE | Bryant Ranch Prepack | 25c0aded-ffcd-4145-a48c-76c5fb220f61 | 2024-08-23 | Warnings, Adverse reactions | 71335-0842-9 71335-0842 71335084209 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.