NDC product
day severe cold night cold and flu
NDC 11822-0717 · Rite Aid Corporation
Key facts
| Product NDC | 11822-0717 |
|---|---|
| Proprietary name | day severe cold night cold and flu |
| Labeler | Rite Aid Corporation |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M012 |
| Marketing start | Jun 28, 2017 |
| Marketing end | Jan 31, 2021 |
| Listing certified through | Jan 31, 2021 |
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: