NDC product
Multivitamin with Fluoride
NDC 75826-170 · WINDER LABORATORIES, LLC
Key facts
| Product NDC | 75826-170 |
|---|---|
| Proprietary name | Multivitamin with Fluoride |
| Nonproprietary name | Sodium Fluoride |
| Substances | SODIUM FLUORIDE, VITAMIN A, ASCORBIC ACID, SODIUM ASCORBATE, CHOLECALCIFEROL, .ALPHA.-TOCOPHEROL ACETATE, DL-, THIAMINE MONONITRATE, RIBOFLAVIN, NIACINAMIDE, PYRIDOXINE HYDROCHLORIDE, FOLIC ACID, CYANOCOBALAMIN |
| Dosage form | TABLET, CHEWABLE |
| Route | ORAL |
| Labeler | WINDER LABORATORIES, LLC |
| Product type | HUMAN PRESCRIPTION DRUG |
| Marketing category | UNAPPROVED DRUG OTHER |
| Pharmacologic classes | Analogs/Derivatives [Chemical/Ingredient], Ascorbic Acid [CS], Vitamin A [CS], Vitamin A [EPC], Vitamin B 12 [CS], Vitamin B 6 [Chemical/Ingredient] and 5 more |
| Marketing start | Dec 1, 2023 |
| Marketing end | Jun 30, 2027 |
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