NDC11 73473090330
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 |
|---|---|
| 73473-0903-30 | 73473-0903 |
| 73473-903-30 | 73473-903 |
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 | MOXIFLOXACIN HYDROCHLORIDE | Solaris Pharma Corporation | 45ce14e5-98b8-296b-e063-6294a90a769b | 2025-09-16 | Boxed warning, Warnings, Adverse reactions | 73473-903-30 73473-903 73473090330 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.