NDC11 50268057613
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 |
|---|---|
| 50268-0576-13 | 50268-0576 |
| 50268-576-13 | 50268-576 |
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 |
|---|---|---|---|---|---|---|
| Moxifloxacin Hydrochloride | MOXIFLOXACIN HYDROCHLORIDE | AvPAK | 371ca7b2-c62d-ef4b-3076-890b385bfff8 | 2026-04-07 | Boxed warning, Warnings, Adverse reactions | 50268-576-13 50268-576 50268057613 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.