NDC product
Tri-Vite Drops with Fluoride
NDC 58657-323 · Method Pharmaceuticals, LLC
Key facts
| Product NDC | 58657-323 |
|---|---|
| Proprietary name | Tri-Vite Drops with Fluoride |
| Nonproprietary name | ASCORBIC ACID, SODIUM FLUORIDE, VITAMIN A and VITAMIN D |
| Substances | VITAMIN A, ASCORBIC ACID, VITAMIN D, SODIUM FLUORIDE |
| Dosage form | SOLUTION |
| Route | ORAL |
| Labeler | Method Pharmaceuticals, LLC |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | UNAPPROVED DRUG OTHER |
| Pharmacologic classes | Ascorbic Acid [CS], Vitamin A [CS], Vitamin A [EPC], Vitamin C [EPC] |
| Marketing start | Jul 25, 2018 |
| 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: