NDC11 70518013300
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 |
|---|---|
| 70518-0133-0 | 70518-0133 |
| 70518-0133-00 | 70518-0133 |
| 70518-133-00 | 70518-133 |
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 |
|---|---|---|---|---|---|---|
| Tizanidine | TIZANIDINE | REMEDYREPACK INC. | 59084f59-9a9b-49f0-a9f4-27f3eab9a228 | 2026-06-23 | Warnings, Adverse reactions | 70518-0133-0 70518-0133 70518013300 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.