NDC11 83324002606
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 |
|---|---|
| 83324-0026-06 | 83324-0026 |
| 83324-0026-6 | 83324-0026 |
| 83324-026-06 | 83324-026 |
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 Maximum Strength Mucus Relief DM 628 | DEXTROMETHORPHAN HBR, GUAIFENESIN | Chain Drug Marketing Association Inc. | a2795bf5-34c6-4de6-b9e5-53a23d18e357 | 2024-04-26 | Warnings | 83324-026-06 83324-026 83324002606 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.