NDC11 60505081301
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 |
|---|---|
| 60505-0813-01 | 60505-0813 |
| 60505-0813-1 | 60505-0813 |
| 60505-813-01 | 60505-813 |
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 |
|---|---|---|---|---|---|---|
| Butorphanol Tartrate | BUTORPHANOL TARTRATE | Apotex Corp. | b8e48063-0b40-ee43-85c1-4ef2de80c404 | 2026-09-09 | Boxed warning, Warnings, Adverse reactions | 60505-0813-1 60505-0813 60505081301 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.