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Nutri-Tab OB - 76331-905-90 - (SODIUM ASCORBATE, CHOLECALCIFEROL, .ALPHA.-TOCOPHEROL ACETATE, D-, THIAMINE MONONITRATE, RIBOFLAVIN, NIACINAMIDE, PYRIDOXINE HYDROCHLORIDE, FOLIC ACID, CYANOCOBALAMIN, CALCIUM FORMATE, CALCIUM CARBONATE, FERROUS BISGLYCINATE, POTASSIUM IODIDE, ZINC OXIDE, CHOLINE BITARTRATE)

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Drug Information of Nutri-Tab OB

Product NDC: 76331-905
Proprietary Name: Nutri-Tab OB
Non Proprietary Name: SODIUM ASCORBATE, CHOLECALCIFEROL, .ALPHA.-TOCOPHEROL ACETATE, D-, THIAMINE MONONITRATE, RIBOFLAVIN, NIACINAMIDE, PYRIDOXINE HYDROCHLORIDE, FOLIC ACID, CYANOCOBALAMIN, CALCIUM FORMATE, CALCIUM CARBONATE, FERROUS BISGLYCINATE, POTASSIUM IODIDE, ZINC OXIDE, CHOLINE BITARTRATE
Active Ingredient(s): 30; 45; 155; 450; 55; 10; 32; 1000; 20; 100; 50; 3; 120; 3; 10    [iU]/1; mg/1; mg/1; [iU]/1; mg/1; ug/1; mg/1; ug/1; mg/1; ug/1; mg/1; mg/1; mg/1; mg/1; mg/1 & nbsp;   SODIUM ASCORBATE, CHOLECALCIFEROL, .ALPHA.-TOCOPHEROL ACETATE, D-, THIAMINE MONONITRATE, RIBOFLAVIN, NIACINAMIDE, PYRIDOXINE HYDROCHLORIDE, FOLIC ACID, CYANOCOBALAMIN, CALCIUM FORMATE, CALCIUM CARBONATE, FERROUS BISGLYCINATE, POTASSIUM IODIDE, ZINC OXIDE, CHOLINE BITARTRATE
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Nutri-Tab OB

Product NDC: 76331-905
Labeler Name: WH Nutritionals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20120503

Package Information of Nutri-Tab OB

Package NDC: 76331-905-90
Package Description: 90 TABLET in 1 BOTTLE, PLASTIC (76331-905-90)

NDC Information of Nutri-Tab OB

NDC Code 76331-905-90
Proprietary Name Nutri-Tab OB
Package Description 90 TABLET in 1 BOTTLE, PLASTIC (76331-905-90)
Product NDC 76331-905
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name SODIUM ASCORBATE, CHOLECALCIFEROL, .ALPHA.-TOCOPHEROL ACETATE, D-, THIAMINE MONONITRATE, RIBOFLAVIN, NIACINAMIDE, PYRIDOXINE HYDROCHLORIDE, FOLIC ACID, CYANOCOBALAMIN, CALCIUM FORMATE, CALCIUM CARBONATE, FERROUS BISGLYCINATE, POTASSIUM IODIDE, ZINC OXIDE, CHOLINE BITARTRATE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120503
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name WH Nutritionals, LLC
Substance Name .ALPHA.-TOCOPHEROL ACETATE, D-; CALCIUM CARBONATE; CALCIUM FORMATE; CHOLECALCIFEROL; CHOLINE BITARTRATE; CYANOCOBALAMIN; FERROUS BISGLYCINATE; FOLIC ACID; NIACINAMIDE; POTASSIUM IODIDE; PYRIDOXINE HYDROCHLORIDE; RIBOFLAVIN; SODIUM ASCORBATE; THIAMINE MONONITRATE; ZINC OXIDE
Strength Number 30; 45; 155; 450; 55; 10; 32; 1000; 20; 100; 50; 3; 120; 3; 10
Strength Unit [iU]/1; mg/1; mg/1; [iU]/1; mg/1; ug/1; mg/1; ug/1; mg/1; ug/1; mg/1; mg/1; mg/1; mg/1; mg/1
Pharmaceutical Classes Vitamin D [Chemical/Ingredient],Vitamin D [EPC],Vitamin B 12 [Chemical/Ingredient],Vitamin B12 [EPC],Blood Coagulation Factor [EPC],Increased Coagulation Factor Activity [PE],Calcium [Chemical/Ingredient],Cations, Divalent [Chemical/Ingredient],Blood Coagulation Factor [EPC],Increased Coagulation Factor Activity [PE],Calcium [Chemical/Ingredient],Cations, Divalent [Chemical/Ingredient]

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