NDC11 69729006204
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 |
|---|---|
| 69729-0062-04 | 69729-0062 |
| 69729-0062-4 | 69729-0062 |
| 69729-062-04 | 69729-062 |
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 HYDROBROMIDE and GUAIFENESIN | DEXTROMETHORPHAN HYDROBROMIDE AND GUAIFENESIN | OPMX LLC | 826c2f47-00a6-4060-a7ad-1ef26ccfddd1 | 2025-05-15 | Warnings | 69729-062-04 69729-062 69729006204 |