NDC11 68382052705
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 |
|---|---|
| 68382-0527-05 | 68382-0527 |
| 68382-0527-5 | 68382-0527 |
| 68382-527-05 | 68382-527 |
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 |
|---|---|---|---|---|---|---|
| bumetanide | BUMETANIDE | Zydus Pharmaceuticals (USA) Inc. | 525138cd-832a-41d0-84b0-83921b12bd2a | 2023-12-05 | Boxed warning, Warnings, Adverse reactions | 68382-527-05 68382-527 68382052705 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.