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Adult Infuvite Multiple Vitamins for Infusion Pharmacy Bulk - 54643-5650-2 - (Asorbic Acid, Vitamin A Palmitate, Cholecalciferol, Thiamine Hydrochloride, Riboflavin 5-phosphate sodium, Pyridoxine Hydrochloride, Niacinamide, Dexpanthenol, Alpha-tocopherol acetate, Vitamin K1, Folic Acid, Biotin, Cyanocobalamin)

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Drug Information of Adult Infuvite Multiple Vitamins for Infusion Pharmacy Bulk

Product NDC: 54643-5650
Proprietary Name: Adult Infuvite Multiple Vitamins for Infusion Pharmacy Bulk
Non Proprietary Name: Asorbic Acid, Vitamin A Palmitate, Cholecalciferol, Thiamine Hydrochloride, Riboflavin 5-phosphate sodium, Pyridoxine Hydrochloride, Niacinamide, Dexpanthenol, Alpha-tocopherol acetate, Vitamin K1, Folic Acid, Biotin, Cyanocobalamin
Active Ingredient(s): 10; 200; 60; 200; 5; 15; 600; 40; 150; 6; 3.6; 6; 3300    [iU]/10mL; mg/10mL; ug/10mL; [iU]/10mL; ug/10mL; mg/10mL; ug/10mL; mg/10mL; ug/10mL; mg/10mL; mg/10mL; mg/10mL; [iU]/10mL & nbsp;   Asorbic Acid, Vitamin A Palmitate, Cholecalciferol, Thiamine Hydrochloride, Riboflavin 5-phosphate sodium, Pyridoxine Hydrochloride, Niacinamide, Dexpanthenol, Alpha-tocopherol acetate, Vitamin K1, Folic Acid, Biotin, Cyanocobalamin
Administration Route(s): INTRAVENOUS
Dosage Form(s): INJECTION, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Adult Infuvite Multiple Vitamins for Infusion Pharmacy Bulk

Product NDC: 54643-5650
Labeler Name: Sandoz Canada Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021559
Marketing Category: NDA
Start Marketing Date: 20030616

Package Information of Adult Infuvite Multiple Vitamins for Infusion Pharmacy Bulk

Package NDC: 54643-5650-2
Package Description: 2 VIAL in 1 CARTON (54643-5650-2) > 50 mL in 1 VIAL

NDC Information of Adult Infuvite Multiple Vitamins for Infusion Pharmacy Bulk

NDC Code 54643-5650-2
Proprietary Name Adult Infuvite Multiple Vitamins for Infusion Pharmacy Bulk
Package Description 2 VIAL in 1 CARTON (54643-5650-2) > 50 mL in 1 VIAL
Product NDC 54643-5650
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Asorbic Acid, Vitamin A Palmitate, Cholecalciferol, Thiamine Hydrochloride, Riboflavin 5-phosphate sodium, Pyridoxine Hydrochloride, Niacinamide, Dexpanthenol, Alpha-tocopherol acetate, Vitamin K1, Folic Acid, Biotin, Cyanocobalamin
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAVENOUS
Start Marketing Date 20030616
Marketing Category Name NDA
Labeler Name Sandoz Canada Inc
Substance Name .ALPHA.-TOCOPHEROL ACETATE; ASCORBIC ACID; BIOTIN; CHOLECALCIFEROL; CYANOCOBALAMIN; DEXPANTHENOL; FOLIC ACID; NIACINAMIDE; PHYTONADIONE; PYRIDOXINE HYDROCHLORIDE; RIBOFLAVIN 5'-PHOSPHATE SODIUM; THIAMINE HYDROCHLORIDE; VITAMIN A PALMITATE
Strength Number 10; 200; 60; 200; 5; 15; 600; 40; 150; 6; 3.6; 6; 3300
Strength Unit [iU]/10mL; mg/10mL; ug/10mL; [iU]/10mL; ug/10mL; mg/10mL; ug/10mL; mg/10mL; ug/10mL; mg/10mL; mg/10mL; mg/10mL; [iU]/10mL
Pharmaceutical Classes Vitamin A [Chemical/Ingredient],Vitamin A [EPC],Vitamin D [Chemical/Ingredient],Vitamin D [EPC],Increased Prothrombin Activity [PE],Reversed Anticoagulation Activity [PE],Vitamin K [Chemical/Ingredient],Vitamin K [EPC],Warfarin Reversal Agent [EPC],Vitamin B 12 [Chemical/Ingredient],Vitamin B12 [EPC]

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