NDC11 70095002602
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 |
|---|---|
| 70095-0026-02 | 70095-0026 |
| 70095-0026-2 | 70095-0026 |
| 70095-026-02 | 70095-026 |
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 |
|---|---|---|---|---|---|---|
| Desmopressin Acetate | DESMOPRESSIN ACETATE | Sun Pharmaceutical Industries Limited | cdec2cc2-4fd9-474e-884f-d0599e40948f | 2023-04-06 | Boxed warning, Warnings, Adverse reactions | 70095-026-02 70095-026 70095002602 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.