NDC11 70095004330
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 |
|---|---|
| 70095-0043-30 | 70095-0043 |
| 70095-043-30 | 70095-043 |
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 |
|---|---|---|---|---|---|---|
| Deflazacort | DEFLAZACORT | Sun Pharmaceutical Industries, Inc. | fb5350d5-ead1-41f4-8b25-0da0bd7fcffe | 2025-12-09 | Warnings, Adverse reactions | 70095-043-30 70095-043 70095004330 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.