NDC product
Up and Up Cold Flu Relief Day Night
NDC 11673-733 · Target Corporation
Key facts
| Product NDC | 11673-733 |
|---|---|
| Proprietary name | Up and Up Cold Flu Relief Day Night |
| Labeler | Target Corporation |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M012 |
| Marketing start | Aug 18, 2014 |
| Marketing end | Apr 1, 2018 |
| Listing certified through | Apr 1, 2018 |
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: