NDC product
Guaifenesin and Dextromethorphan HBr
NDC 41415-998 · PUBLIX SUPER MARKETS, INC
Key facts
| Product NDC | 41415-998 |
|---|---|
| Proprietary name | Guaifenesin and Dextromethorphan HBr |
| Nonproprietary name | Guaifenesin and Dextromethorphan Hbr |
| Substances | GUAIFENESIN, DEXTROMETHORPHAN HYDROBROMIDE |
| Dosage form | TABLET, EXTENDED RELEASE |
| Route | ORAL |
| Labeler | PUBLIX SUPER MARKETS, INC |
| Product type | HUMAN OTC DRUG |
| Marketing category | ANDA |
| Application number | ANDA214781 |
| 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 | Jul 1, 2021 |
| 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: