NDC11 83324021704
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 |
|---|---|
| 83324-0217-04 | 83324-0217 |
| 83324-0217-4 | 83324-0217 |
| 83324-217-04 | 83324-217 |
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 |
|---|---|---|---|---|---|---|
| QUALITY CHOICE Anti-Nausea | DEXTROSE(GLUCOSE),LEVULOSE(FRUCTOSE),PHOSPHORIC ACID | QUALITY CHOICE (CHAIN DRUG MARKETING ASSOCIATION) | 68207fa3-3f69-4405-9191-be702e1bf520 | 2025-12-04 | Warnings | 83324-217-04 83324-217 83324021704 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.