NDC product
fluorodine ACTIVE fresh Fluoride Anticavity
NDC 22912-001 · Multibrands International Ltd
Key facts
| Product NDC | 22912-001 |
|---|---|
| Proprietary name | fluorodine ACTIVE fresh Fluoride Anticavity |
| Labeler | Multibrands International Ltd |
| Marketing category | OTC MONOGRAPH FINAL |
| Application number | part355 |
| Marketing start | Mar 27, 2013 |
| Marketing end | Jan 7, 2016 |
| Listing certified through | Jan 7, 2016 |
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: