NDC11 73086021001
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 |
|---|---|
| 73086-0210-01 | 73086-0210 |
| 73086-0210-1 | 73086-0210 |
| 73086-210-01 | 73086-210 |
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 |
|---|---|---|---|---|---|---|
| ibuprofen | IBUPROFEN | SKYA HEALTH, LLC | 1c28af16-7246-4e4c-a1be-939655c37242 | 2024-05-31 | Boxed warning, Warnings, Adverse reactions | 73086-210-01 73086-210 73086021001 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.