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Multi-Vit with Fluoride and Iron - 0603-1452-47 - (vitamin a palmitate and ascorbic acid and cholecalciferol and .alpha.-tocopherol acetate, dl- and thiamine hydrochloride and riboflavin and niacinamide and pyridoxine hydrochloride and ferrous sulfate and sodium fluoride solution)

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Drug Information of Multi-Vit with Fluoride and Iron

Product NDC: 0603-1452
Proprietary Name: Multi-Vit with Fluoride and Iron
Non Proprietary Name: vitamin a palmitate and ascorbic acid and cholecalciferol and .alpha.-tocopherol acetate, dl- and thiamine hydrochloride and riboflavin and niacinamide and pyridoxine hydrochloride and ferrous sulfate and sodium fluoride solution
Active Ingredient(s): 5; 35; 400; 10; 8; .4; .6; .25; .5; 1500    [iU]/mL; mg/mL; [iU]/mL; mg/mL; mg/mL; mg/mL; mg/mL; mg/mL; mg/mL; [iU]/mL & nbsp;   vitamin a palmitate and ascorbic acid and cholecalciferol and .alpha.-tocopherol acetate, dl- and thiamine hydrochloride and riboflavin and niacinamide and pyridoxine hydrochloride and ferrous sulfate and sodium fluoride solution
Administration Route(s): ORAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Multi-Vit with Fluoride and Iron

Product NDC: 0603-1452
Labeler Name: Qualitest Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 19980107

Package Information of Multi-Vit with Fluoride and Iron

Package NDC: 0603-1452-47
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON (0603-1452-47) > 50 mL in 1 BOTTLE, PLASTIC

NDC Information of Multi-Vit with Fluoride and Iron

NDC Code 0603-1452-47
Proprietary Name Multi-Vit with Fluoride and Iron
Package Description 1 BOTTLE, PLASTIC in 1 CARTON (0603-1452-47) > 50 mL in 1 BOTTLE, PLASTIC
Product NDC 0603-1452
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name vitamin a palmitate and ascorbic acid and cholecalciferol and .alpha.-tocopherol acetate, dl- and thiamine hydrochloride and riboflavin and niacinamide and pyridoxine hydrochloride and ferrous sulfate and sodium fluoride solution
Dosage Form Name SOLUTION
Route Name ORAL
Start Marketing Date 19980107
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Qualitest Pharmaceuticals
Substance Name .ALPHA.-TOCOPHEROL ACETATE, DL-; ASCORBIC ACID; CHOLECALCIFEROL; FERROUS SULFATE; NIACINAMIDE; PYRIDOXINE HYDROCHLORIDE; RIBOFLAVIN; SODIUM FLUORIDE; THIAMINE HYDROCHLORIDE; VITAMIN A PALMITATE
Strength Number 5; 35; 400; 10; 8; .4; .6; .25; .5; 1500
Strength Unit [iU]/mL; mg/mL; [iU]/mL; mg/mL; mg/mL; mg/mL; mg/mL; mg/mL; mg/mL; [iU]/mL
Pharmaceutical Classes Vitamin A [Chemical/Ingredient],Vitamin A [EPC],Vitamin D [Chemical/Ingredient],Vitamin D [EPC]

Complete Information of Multi-Vit with Fluoride and Iron


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