"76439-258-50" National Drug Code (NDC)

Preplus 500 TABLET in 1 BOTTLE (76439-258-50)
(Virtus Pharmaceuticals LLC)

NDC Code76439-258-50
Package Description500 TABLET in 1 BOTTLE (76439-258-50)
Product NDC76439-258
Product Type NameHUMAN PRESCRIPTION DRUG
Proprietary NamePreplus
Non-Proprietary Name.beta.-carotene, Ascorbic Acid, Cholecalciferol, .alpha.-tocopherol Acetate, Dl-, Thiamine Mononitrate, Riboflavin, Niacinamide, Pyridoxine Hydrochloride, Folic Acid, Cyanocobalamin, Calcium Carbonate, Ferrous Fumarate, Zinc Oxide And Cupric Oxide
Dosage FormTABLET
UsageORAL
Start Marketing Date20140404
Marketing Category NameUNAPPROVED DRUG OTHER
ManufacturerVirtus Pharmaceuticals LLC
Substance Name.BETA.-CAROTENE; ASCORBIC ACID; CHOLECALCIFEROL; .ALPHA.-TOCOPHEROL ACETATE, DL-; THIAMINE MONONITRATE; RIBOFLAVIN; NIACINAMIDE; PYRIDOXINE HYDROCHLORIDE; FOLIC ACID; CYANOCOBALAMIN; CALCIUM CARBONATE; FERROUS FUMARATE; ZINC OXIDE; CUPRIC OXIDE
Strength4000; 120; 400; 22; 1.84; 3; 20; 10; 1; 12; 200; 27; 25; 2
Strength Unit[iU]/1; mg/1; [iU]/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; ug/1; mg/1; mg/1; mg/1; mg/1
Pharmacy ClassesVitamin D [Chemical/Ingredient],Vitamin D [EPC],Vitamin B6 Analog [EPC],Vitamin B 6 [Chemical/Ingredient],Analogs/Derivatives [Chemical/Ingredient],Vitamin B 12 [Chemical/Ingredient],Vitamin B12 [EPC],Blood Coagulation Factor [EPC],Increased Coagulation Factor Activity [PE],Calcium [Chemical/Ingredient],Cations, Divalent [Chemical/Ingredient],Copper Absorption Inhibitor [EPC],Decreased Copper Ion Absorption [PE]

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