NDC product
Maxi-Tuss AC
NDC 58605-313 · MCR American Pharmaceuticals, Inc.
Key facts
| Product NDC | 58605-313 |
|---|---|
| Proprietary name | Maxi-Tuss AC |
| Labeler | MCR American Pharmaceuticals, Inc. |
| Marketing category | OTC MONOGRAPH FINAL |
| Application number | part341 |
| Marketing start | Aug 1, 2020 |
| Listing certified through | Dec 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: