NDC11 68210080001
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 |
|---|---|
| 68210-0800-01 | 68210-0800 |
| 68210-0800-1 | 68210-0800 |
| 68210-800-01 | 68210-800 |
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 |
|---|---|---|---|---|---|---|
| VALUMEDS IBUPROFEN | IBUPROFEN | SPIRIT PHARMACEUTICALS LLC | a6d4ceb0-2b79-496a-aa1e-27edd507ced0 | 2024-12-10 | Warnings | 68210-0800-1 68210-0800 68210080001 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.