NDC11 83324002504
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 |
|---|---|
| 83324-0025-04 | 83324-0025 |
| 83324-0025-4 | 83324-0025 |
| 83324-025-04 | 83324-025 |
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 |
|---|---|---|---|---|---|---|
| QCH Adult Tussin DM Sugar free 545 | DEXTROMETHORPHAN HBR, GUAIFENESIN | Chain Drug Marketing Association Inc. | 17cb91f0-32ec-9e0f-e063-6394a90a0509 | 2024-05-08 | Warnings | 83324-025-04 83324-025 83324002504 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.