Product NDC: | 0603-1786 |
Proprietary Name: | Tri-Vit with Fluoride Drops |
Non Proprietary Name: | ascorbic acid and chlolecalciferol and sodium fluorideand vitamin A plamitate |
Active Ingredient(s): | 35; 400; .5; 1500 mg/mL; [iU]/mL; mg/mL; [iU]/mL & nbsp; ascorbic acid and chlolecalciferol and sodium fluorideand vitamin A plamitate |
Administration Route(s): | ORAL |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0603-1786 |
Labeler Name: | Qualitest Pharmaceuticals |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 19950401 |
Package NDC: | 0603-1786-47 |
Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (0603-1786-47) > 50 mL in 1 BOTTLE, PLASTIC |
NDC Code | 0603-1786-47 |
Proprietary Name | Tri-Vit with Fluoride Drops |
Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (0603-1786-47) > 50 mL in 1 BOTTLE, PLASTIC |
Product NDC | 0603-1786 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | ascorbic acid and chlolecalciferol and sodium fluorideand vitamin A plamitate |
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; .5; 1500 |
Strength Unit | mg/mL; [iU]/mL; mg/mL; [iU]/mL |
Pharmaceutical Classes | Vitamin D [Chemical/Ingredient],Vitamin D [EPC] |