Vitafol - 0642-0092-01 - (Omega-3 Fatty Acids, Niacin, .Alpha.-Tocopherol, Vitamin D, Lauric Acid, Vitamin A, Ascorbic Acid, Thiamine Mononitrate, Riboflavin, Pyridoxine Hydrochloride, Cyanocobalamin, Iron, Zinc, Copper, Iodine, Magnesium, and Folic Acid)

Alphabetical Index


Drug Information of Vitafol

Product NDC: 0642-0092
Proprietary Name: Vitafol
Non Proprietary Name: Omega-3 Fatty Acids, Niacin, .Alpha.-Tocopherol, Vitamin D, Lauric Acid, Vitamin A, Ascorbic Acid, Thiamine Mononitrate, Riboflavin, Pyridoxine Hydrochloride, Cyanocobalamin, Iron, Zinc, Copper, Iodine, Magnesium, and Folic Acid
Active Ingredient(s): 10; 12; 2; 12; 1; 200; 27; 60; 5; 15; 200; 2.5; 1.8; 1.6; 1100; 1000; 15    [iU]/1; mg/1; mg/1; ug/1; mg/1; ug/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; [iU]/1; [iU]/1; mg/1 & nbsp;   Omega-3 Fatty Acids, Niacin, .Alpha.-Tocopherol, Vitamin D, Lauric Acid, Vitamin A, Ascorbic Acid, Thiamine Mononitrate, Riboflavin, Pyridoxine Hydrochloride, Cyanocobalamin, Iron, Zinc, Copper, Iodine, Magnesium, and Folic Acid
Administration Route(s): ORAL
Dosage Form(s): CAPSULE, LIQUID FILLED
Coding System: National Drug Codes(NDC)

Labeler Information of Vitafol

Product NDC: 0642-0092
Labeler Name: Everett Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20120423

Package Information of Vitafol

Package NDC: 0642-0092-01
Package Description: 1 BLISTER PACK in 1 BOX (0642-0092-01) > 4 CAPSULE, LIQUID FILLED in 1 BLISTER PACK

NDC Information of Vitafol

NDC Code 0642-0092-01
Proprietary Name Vitafol
Package Description 1 BLISTER PACK in 1 BOX (0642-0092-01) > 4 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
Product NDC 0642-0092
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Omega-3 Fatty Acids, Niacin, .Alpha.-Tocopherol, Vitamin D, Lauric Acid, Vitamin A, Ascorbic Acid, Thiamine Mononitrate, Riboflavin, Pyridoxine Hydrochloride, Cyanocobalamin, Iron, Zinc, Copper, Iodine, Magnesium, and Folic Acid
Dosage Form Name CAPSULE, LIQUID FILLED
Route Name ORAL
Start Marketing Date 20120423
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Everett Laboratories, Inc.
Substance Name .ALPHA.-TOCOPHEROL; ASCORBIC ACID; COPPER; CYANOCOBALAMIN; FOLIC ACID; IODINE; IRON; LAURIC ACID; MAGNESIUM; NIACIN; OMEGA-3 FATTY ACIDS; PYRIDOXINE HYDROCHLORIDE; RIBOFLAVIN; THIAMINE MONONITRATE; VITAMIN A; VITAMIN D; ZINC
Strength Number 10; 12; 2; 12; 1; 200; 27; 60; 5; 15; 200; 2.5; 1.8; 1.6; 1100; 1000; 15
Strength Unit [iU]/1; mg/1; mg/1; ug/1; mg/1; ug/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; [iU]/1; [iU]/1; mg/1
Pharmaceutical Classes Vitamin D [Chemical/Ingredient],Vitamin D [EPC],Vitamin B 12 [Chemical/Ingredient],Vitamin B12 [EPC]

Complete Information of Vitafol


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