NDC11 75987007009
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 |
|---|---|
| 75987-0070-09 | 75987-0070 |
| 75987-0070-9 | 75987-0070 |
| 75987-070-09 | 75987-070 |
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 |
|---|---|---|---|---|---|---|
| BUPHENYL | SODIUM PHENYLBUTYRATE | Horizon Therapeutics USA, Inc. | 463a36fa-3eb2-4326-8bd0-c8c7a11bca3a | 2024-10-30 | Warnings, Adverse reactions | 75987-070-09 75987-070 75987007009 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.