NDC11 84415001101
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 |
|---|---|
| 84415-0011-01 | 84415-0011 |
| 84415-0011-1 | 84415-0011 |
| 84415-011-01 | 84415-011 |
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 |
|---|---|---|---|---|---|---|
| Dextromethorphan HBr. and Guaifenesin | DEXTROMETHORPHAN HBR. AND GUAIFENESIN | Everpharm LLC | 0c7cd5c4-459d-4e42-ae22-b94f2e29cffb | 2025-01-16 | Warnings | 84415-011-01 84415-011 84415001101 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.