NDC product
Sodium Fluoride 5000 ppm Fruit
NDC 11527-730 · Sheffield Pharmaceuticals LLC
Key facts
| Product NDC | 11527-730 |
|---|---|
| Proprietary name | Sodium Fluoride 5000 ppm Fruit |
| Nonproprietary name | Sodium Fluoride |
| Substances | SODIUM FLUORIDE |
| Dosage form | PASTE, DENTIFRICE |
| Route | DENTAL |
| Labeler | Sheffield Pharmaceuticals LLC |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | UNAPPROVED DRUG OTHER |
| Marketing start | Mar 26, 2020 |
| 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: