NDC11 70095005701
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 |
|---|---|
| 70095-0057-01 | 70095-0057 |
| 70095-0057-1 | 70095-0057 |
| 70095-057-01 | 70095-057 |
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 |
|---|---|---|---|---|---|---|
| Pomalidomide | POMALIDOMIDE | Sun Pharmaceutical Industries, Inc. | 3c222961-5398-4185-b2d0-defe90230094 | 2026-09-01 | Boxed warning, Warnings, Adverse reactions | 70095-057-01 70095-057 70095005701 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.