NDC product
DEXTROMETHORPHAN HYDROBROMIDE and GUAIFENESIN
NDC 69729-812 · OPMX LLC
Key facts
| Product NDC | 69729-812 |
|---|---|
| Proprietary name | DEXTROMETHORPHAN HYDROBROMIDE and GUAIFENESIN |
| Nonproprietary name | DEXTROMETHORPHAN HYDROBROMIDE and GUAIFENESIN |
| Substances | DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN |
| Dosage form | SYRUP |
| Route | ORAL |
| Labeler | OPMX LLC |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M012 |
| Pharmacologic classes | Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE], Sigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA], Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC] and 1 more |
| Marketing start | Oct 15, 2025 |
| Listing certified through | Dec 31, 2027 |
At a glance
- 1–9 Package NDCs
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About National Drug Codes (NDC)
The National Drug Code (NDC) is the FDA's product identifier for drugs; the product NDC identifies the labeler and product, and each package adds a package code.
Source: U.S. Food and Drug Administration (FDA), National Drug Code Directory · Source date: