NDC11 65197029712
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 |
|---|---|
| 65197-0297-12 | 65197-0297 |
| 65197-297-12 | 65197-297 |
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 |
|---|---|---|---|---|---|---|
| BONINE | MECLIZINE HYDROCHLORIDE | WellSpring Pharmaceutical Corporation | 0b2ea6b8-b342-4940-8922-898758fbeb31 | 2025-03-21 | Warnings | 65197-297-12 65197-297 65197029712 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.