NDC product
Clinpro 5000
NDC 48878-3120 · Solventum US LLC
Key facts
| Product NDC | 48878-3120 |
|---|---|
| Proprietary name | Clinpro 5000 |
| Nonproprietary name | sodium fluoride |
| Substances | SODIUM FLUORIDE |
| Dosage form | PASTE, DENTIFRICE |
| Route | ORAL |
| Labeler | Solventum US LLC |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | UNAPPROVED DRUG OTHER |
| Marketing start | Jan 1, 2009 |
| Listing certified through | Dec 31, 2026 |
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: