NDC11 00781305670
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 |
|---|---|
| 00781-3056-70 | 00781-3056 |
| 0781-3056-70 | 0781-3056 |
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 |
|---|---|---|---|---|---|---|
| Isoniazid | ISONIAZID | Sandoz Inc | 77795c31-1cdf-4a20-b4a1-cd15f5b310f1 | 2025-02-24 | Boxed warning, Warnings, Adverse reactions | 0781-3056-70 0781-3056 00781305670 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.