NDC11 50580020902
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 |
|---|---|
| 50580-0209-02 | 50580-0209 |
| 50580-0209-2 | 50580-0209 |
| 50580-209-02 | 50580-209 |
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 |
|---|---|---|---|---|---|---|
| TYLENOL Extra Strength | ACETAMINOPHEN | Kenvue Brands LLC | ab02080a-c903-4e4a-a9f3-2b8197ed2f2b | 2025-09-17 | Warnings | 50580-209-02 50580-209 50580020902 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.