NDC11 42291062401
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 |
|---|---|
| 42291-0624-01 | 42291-0624 |
| 42291-0624-1 | 42291-0624 |
| 42291-624-01 | 42291-624 |
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 |
|---|---|---|---|---|---|---|
| Mexiletine Hydrochloride | MEXILETINE HYDROCHLORIDE | AvKARE | c528aae3-ff51-b9e4-a401-4ef5910e4b43 | 2026-01-15 | Boxed warning, Adverse reactions | 42291-624-01 42291-624 42291062401 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.