NDC11 58602061005
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 |
|---|---|
| 58602-0610-05 | 58602-0610 |
| 58602-0610-5 | 58602-0610 |
| 58602-610-05 | 58602-610 |
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 |
|---|---|---|---|---|---|---|
| DEXTROMETHORPHAN POLISTIREX | DEXTROMETHORPHAN POLISTIREX | Aurohealth LLC | 4fde00af-3824-44f1-8a5f-d88518e0a8c8 | 2026-05-04 | Warnings | 58602-610-05 58602-610 58602061005 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.