NDC11 62175047241
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 |
|---|---|
| 62175-0472-41 | 62175-0472 |
| 62175-472-41 | 62175-472 |
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 |
|---|---|---|---|---|---|---|
| Paroxetine Hydrochloride | PAROXETINE HYDROCHLORIDE | Lannett Company, Inc. | f22886f5-230c-47e4-9dd8-ffb14c8d6ae4 | 2023-08-22 | Boxed warning, Warnings, Adverse reactions | 62175-472-41 62175-472 62175047241 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.