NDC product
Nighttime Cold and Flu Relief
NDC 83324-163 · QUALITY CHOICE (Chain Drug Marketing Association)
Key facts
| Product NDC | 83324-163 |
|---|---|
| Proprietary name | Nighttime Cold and Flu Relief |
| Nonproprietary name | Acetaminophen Dextromethorphan HBr Doxylamine Succinate |
| Substances | ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE |
| Dosage form | LIQUID |
| Route | ORAL |
| Labeler | QUALITY CHOICE (Chain Drug Marketing Association) |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M012 |
| Pharmacologic classes | Antihistamine [EPC], Histamine Receptor Antagonists [MoA], Sigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA], Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC], Uncompetitive NMDA Receptor Antagonists [MoA] |
| Marketing start | Jul 31, 2024 |
| 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: