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Multivitamin with Fluoride - 59088-109-59 - (Sodium Fluoride)

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Drug Information of Multivitamin with Fluoride

Product NDC: 59088-109
Proprietary Name: Multivitamin with Fluoride
Non Proprietary Name: Sodium Fluoride
Active Ingredient(s): 15; 24; 400; 4.5; 300; 13.5; 1.05; 1.2; 36; 1; 1.05; 2500    [iU]/1; mg/1; [iU]/1; ug/1; ug/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; [iU]/1 & nbsp;   Sodium Fluoride
Administration Route(s): ORAL
Dosage Form(s): TABLET, CHEWABLE
Coding System: National Drug Codes(NDC)

Labeler Information of Multivitamin with Fluoride

Product NDC: 59088-109
Labeler Name: PureTek Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20110601

Package Information of Multivitamin with Fluoride

Package NDC: 59088-109-59
Package Description: 100 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (59088-109-59)

NDC Information of Multivitamin with Fluoride

NDC Code 59088-109-59
Proprietary Name Multivitamin with Fluoride
Package Description 100 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (59088-109-59)
Product NDC 59088-109
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Sodium Fluoride
Dosage Form Name TABLET, CHEWABLE
Route Name ORAL
Start Marketing Date 20110601
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name PureTek Corporation
Substance Name .ALPHA.-TOCOPHEROL ACETATE, DL-; ASCORBIC ACID; CHOLECALCIFEROL; CYANOCOBALAMIN; FOLIC ACID; NIACINAMIDE; PYRIDOXINE HYDROCHLORIDE; RIBOFLAVIN; SODIUM ASCORBATE; SODIUM FLUORIDE; THIAMINE MONONITRATE; VITAMIN A
Strength Number 15; 24; 400; 4.5; 300; 13.5; 1.05; 1.2; 36; 1; 1.05; 2500
Strength Unit [iU]/1; mg/1; [iU]/1; ug/1; ug/1; mg/1; mg/1; mg/1; mg/1; mg/1; mg/1; [iU]/1
Pharmaceutical Classes Vitamin A [Chemical/Ingredient],Vitamin A [EPC],Vitamin D [Chemical/Ingredient],Vitamin D [EPC],Vitamin B 12 [Chemical/Ingredient],Vitamin B12 [EPC]

Complete Information of Multivitamin with Fluoride


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