NDC11 82667020005
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 |
|---|---|
| 82667-0200-05 | 82667-0200 |
| 82667-0200-5 | 82667-0200 |
| 82667-200-05 | 82667-200 |
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 |
|---|---|---|---|---|---|---|
| IOPIDINE 1% | APRACLONIDINE HYDROCHLORIDE OPHTHALMIC SOLUTION | Harrow Eye, LLC | 00f18845-ccde-8678-e063-6294a90a3374 | 2026-05-08 | Warnings, Adverse reactions | 82667-200-05 82667-200 82667020005 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.