NDC product
Dextromethorphan HBr and Guaifenesin Oral Solution
NDC 81033-103 · KESIN PHARMA CORPORATION
Key facts
| Product NDC | 81033-103 |
|---|---|
| Proprietary name | Dextromethorphan HBr and Guaifenesin Oral Solution |
| Nonproprietary name | Dextromethorphan HBr and Guaifenesin Oral Solution |
| Substances | GUAIFENESIN, DEXTROMETHORPHAN HYDROBROMIDE |
| Dosage form | LIQUID |
| Route | ORAL |
| Labeler | KESIN PHARMA CORPORATION |
| 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 | Dec 2, 2024 |
| Listing certified through | Dec 31, 2026 |
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: