NDC11 63187061421
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 |
|---|---|
| 63187-0614-21 | 63187-0614 |
| 63187-614-21 | 63187-614 |
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 |
|---|---|---|---|---|---|---|
| IBU | IBUPROFEN | Proficient Rx LP | a7098fa1-b5ae-485e-ada9-64154f81fb6a | 2025-12-01 | Boxed warning, Warnings, Adverse reactions | 63187-614-21 63187-614 63187061421 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.