| Product NDC: | 0603-1785 |
| Proprietary Name: | Tri-Vit with Fluoride Drops |
| Non Proprietary Name: | ascorbic acid and cholecalciferol and sodium fluoride and vitamin A palmitate |
| Active Ingredient(s): | 35; 400; .25; 1500 mg/mL; [iU]/mL; mg/mL; [iU]/mL & nbsp; ascorbic acid and cholecalciferol and sodium fluoride and vitamin A palmitate |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 0603-1785 |
| Labeler Name: | Qualitest Pharmaceuticals |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 19950401 |
| Package NDC: | 0603-1785-47 |
| Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (0603-1785-47) > 50 mL in 1 BOTTLE, PLASTIC |
| NDC Code | 0603-1785-47 |
| Proprietary Name | Tri-Vit with Fluoride Drops |
| Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (0603-1785-47) > 50 mL in 1 BOTTLE, PLASTIC |
| Product NDC | 0603-1785 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ascorbic acid and cholecalciferol and sodium fluoride and vitamin A palmitate |
| Dosage Form Name | SOLUTION |
| Route Name | ORAL |
| Start Marketing Date | 19950401 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Qualitest Pharmaceuticals |
| Substance Name | ASCORBIC ACID; CHOLECALCIFEROL; SODIUM FLUORIDE; VITAMIN A PALMITATE |
| Strength Number | 35; 400; .25; 1500 |
| Strength Unit | mg/mL; [iU]/mL; mg/mL; [iU]/mL |
| Pharmaceutical Classes | Vitamin D [Chemical/Ingredient],Vitamin D [EPC] |