NDC11 42708010230
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 |
|---|---|
| 42708-0102-30 | 42708-0102 |
| 42708-102-30 | 42708-102 |
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 |
|---|---|---|---|---|---|---|
| Meclizine Hydrocloride | MECLIZINE HYDROCLORIDE | QPharma Inc | aa0fb895-a867-4482-9bc2-16eee8bfaaa0 | 2025-12-04 | Warnings, Adverse reactions | 42708-102-30 42708-102 42708010230 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.