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Tri-Vitamin with Fluoride
Tri-Vitamin with Fluoride - 44946-1035-8 - (Vitamin A, Ascorbic Acid, Vitamin D, and Sodium Fluoride)
Drug Information of Tri-Vitamin with Fluoride
| Product NDC: | 44946-1035 |
| Proprietary Name: | Tri-Vitamin with Fluoride |
| Non Proprietary Name: | Vitamin A, Ascorbic Acid, Vitamin D, and Sodium Fluoride |
| Active Ingredient(s): | 35; .25; 1500; 400 mg/mL; mg/mL; [iU]/mL; [iU]/mL & nbsp; Vitamin A, Ascorbic Acid, Vitamin D, and Sodium Fluoride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION/ DROPS |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Tri-Vitamin with Fluoride
| Product NDC: | 44946-1035 |
| Labeler Name: | Sancilio & Company Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20111220 |
Package Information of Tri-Vitamin with Fluoride
| Package NDC: | 44946-1035-8 |
| Package Description: | 1 BOTTLE, PLASTIC in 1 CARTON (44946-1035-8) > 50 mL in 1 BOTTLE, PLASTIC |
NDC Information of Tri-Vitamin with Fluoride
| NDC Code | 44946-1035-8 |
| Proprietary Name | Tri-Vitamin with Fluoride |
| Package Description | 1 BOTTLE, PLASTIC in 1 CARTON (44946-1035-8) > 50 mL in 1 BOTTLE, PLASTIC |
| Product NDC | 44946-1035 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Vitamin A, Ascorbic Acid, Vitamin D, and Sodium Fluoride |
| Dosage Form Name | SOLUTION/ DROPS |
| Route Name | ORAL |
| Start Marketing Date | 20111220 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Sancilio & Company Inc |
| Substance Name | ASCORBIC ACID; SODIUM FLUORIDE; VITAMIN A; VITAMIN D |
| Strength Number | 35; .25; 1500; 400 |
| Strength Unit | mg/mL; mg/mL; [iU]/mL; [iU]/mL |
| Pharmaceutical Classes | Vitamin A [Chemical/Ingredient],Vitamin A [EPC] |
