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O-Cal FA multivitamin - 0813-9616-01 - (VITAMIN A ACETATE, Ascorbic Acid, Cholecalciferol, .ALPHA.-TOCOPHEROL ACETATE, THIAMINE MONONITRATE, Riboflavin, Niacin, Pyridoxine, Folic Acid, Cyanocobalamin, CALCIUM CARBONATE, FERROUS FUMARATE, Iodine, Magnesium, Zinc, Copper, and Sodium Fluoride)

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Drug Information of O-Cal FA multivitamin

Product NDC: 0813-9616
Proprietary Name: O-Cal FA multivitamin
Non Proprietary Name: VITAMIN A ACETATE, Ascorbic Acid, Cholecalciferol, .ALPHA.-TOCOPHEROL ACETATE, THIAMINE MONONITRATE, Riboflavin, Niacin, Pyridoxine, Folic Acid, Cyanocobalamin, CALCIUM CARBONATE, FERROUS FUMARATE, Iodine, Magnesium, Zinc, Copper, and Sodium Fluoride
Active Ingredient(s): 30; 90; 200; 400; 2; 12; 27; 1; 150; 100; 20; 4; 3; .5; 3; 2500; 15    [iU]/1; mg/1; mg/1; [iU]/1; mg/1; ug/1; mg/1; mg/1; ug/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; [iU]/1; mg/1 & nbsp;   VITAMIN A ACETATE, Ascorbic Acid, Cholecalciferol, .ALPHA.-TOCOPHEROL ACETATE, THIAMINE MONONITRATE, Riboflavin, Niacin, Pyridoxine, Folic Acid, Cyanocobalamin, CALCIUM CARBONATE, FERROUS FUMARATE, Iodine, Magnesium, Zinc, Copper, and Sodium Fluoride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of O-Cal FA multivitamin

Product NDC: 0813-9616
Labeler Name: Pharmics, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 19700115

Package Information of O-Cal FA multivitamin

Package NDC: 0813-9616-01
Package Description: 100 TABLET in 1 BOTTLE (0813-9616-01)

NDC Information of O-Cal FA multivitamin

NDC Code 0813-9616-01
Proprietary Name O-Cal FA multivitamin
Package Description 100 TABLET in 1 BOTTLE (0813-9616-01)
Product NDC 0813-9616
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name VITAMIN A ACETATE, Ascorbic Acid, Cholecalciferol, .ALPHA.-TOCOPHEROL ACETATE, THIAMINE MONONITRATE, Riboflavin, Niacin, Pyridoxine, Folic Acid, Cyanocobalamin, CALCIUM CARBONATE, FERROUS FUMARATE, Iodine, Magnesium, Zinc, Copper, and Sodium Fluoride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19700115
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Pharmics, Inc.
Substance Name .ALPHA.-TOCOPHEROL ACETATE; ASCORBIC ACID; CALCIUM CARBONATE; CHOLECALCIFEROL; COPPER; CYANOCOBALAMIN; FERROUS FUMARATE; FOLIC ACID; IODINE; MAGNESIUM; NIACIN; PYRIDOXINE; RIBOFLAVIN; SODIUM FLUORIDE; THIAMINE MONONITRATE; VITAMIN A ACETATE; ZINC
Strength Number 30; 90; 200; 400; 2; 12; 27; 1; 150; 100; 20; 4; 3; .5; 3; 2500; 15
Strength Unit [iU]/1; mg/1; mg/1; [iU]/1; mg/1; ug/1; mg/1; mg/1; ug/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; [iU]/1; mg/1
Pharmaceutical Classes Vitamin A [Chemical/Ingredient],Vitamin A [EPC],Vitamin D [Chemical/Ingredient],Vitamin D [EPC],Nicotinic Acid [EPC],Nicotinic Acids [Chemical/Ingredient],Vitamin B 12 [Chemical/Ingredient],Vitamin B12 [EPC],Copper [Chemical/Ingredient],Copper-containing Intrauterine Device [EPC],Decreased Embryonic Implantation [PE],Decreased Sperm Motility [PE],Inhibit Ovum Fertilization [PE]

Complete Information of O-Cal FA multivitamin


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