NDC11 80513042102
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 |
|---|---|
| 80513-0421-02 | 80513-0421 |
| 80513-0421-2 | 80513-0421 |
| 80513-421-02 | 80513-421 |
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 | MECLIZINE HYDROCHLORIDE | Advanced Rx LLC | b0a2a1f7-354e-48bd-9e98-9207bf9f53fd | 2024-11-27 | Warnings | 80513-421-02 80513-421 80513042102 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.