NDC product
Daytime and Nighttime High Blood Pressure Cold and Flu Liquid
NDC 51316-666 · CVS Pharmacy, Inc.
Key facts
| Product NDC | 51316-666 |
|---|---|
| Proprietary name | Daytime and Nighttime High Blood Pressure Cold and Flu Liquid |
| Nonproprietary name | Acetaminophen, Dextromethorphan HBr and Acetaminophen, Dextromethorphan HBr, Doxylamine succinate |
| Dosage form | KIT |
| Route | ORAL |
| Labeler | CVS Pharmacy, Inc. |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M012 |
| Marketing start | Apr 21, 2025 |
| 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: