NDC product
Topco Associates LLC Maximum Strength
NDC 36800-481 · Topco Associates LLC
Key facts
| Product NDC | 36800-481 |
|---|---|
| Proprietary name | Topco Associates LLC |
| Nonproprietary name | Fluoride |
| Substances | SODIUM FLUORIDE, POTASSIUM NITRATE |
| Dosage form | PASTE, DENTIFRICE |
| Route | DENTAL |
| Labeler | Topco Associates LLC |
| Product type | HUMAN OTC DRUG |
| Marketing category | OTC MONOGRAPH DRUG |
| Application number | M022 |
| Marketing start | Jan 20, 2011 |
| Marketing end | Jun 26, 2028 |
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