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Multi Vitamin and Fluoride - 51862-162-50 - (Multivitamin and Fluoride)

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Drug Information of Multi Vitamin and Fluoride

Product NDC: 51862-162
Proprietary Name: Multi Vitamin and Fluoride
Non Proprietary Name: Multivitamin and Fluoride
Active Ingredient(s): 5; 35; 400; 2; 8; .4; .6; .5; .5; 1500    [iU]/mL; mg/mL; [iU]/mL; ug/mL; mg/mL; mg/mL; mg/mL; mg/mL; mg/mL; [iU]/mL & nbsp;   Multivitamin and Fluoride
Administration Route(s): ORAL
Dosage Form(s): SOLUTION/ DROPS
Coding System: National Drug Codes(NDC)

Labeler Information of Multi Vitamin and Fluoride

Product NDC: 51862-162
Labeler Name: Libertas Pharma, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20110521

Package Information of Multi Vitamin and Fluoride

Package NDC: 51862-162-50
Package Description: 1 BOTTLE in 1 CARTON (51862-162-50) > 50 mL in 1 BOTTLE

NDC Information of Multi Vitamin and Fluoride

NDC Code 51862-162-50
Proprietary Name Multi Vitamin and Fluoride
Package Description 1 BOTTLE in 1 CARTON (51862-162-50) > 50 mL in 1 BOTTLE
Product NDC 51862-162
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Multivitamin and Fluoride
Dosage Form Name SOLUTION/ DROPS
Route Name ORAL
Start Marketing Date 20110521
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Libertas Pharma, Inc.
Substance Name ALPHA-TOCOPHEROL; ASCORBIC ACID; CHOLECALCIFEROL; CYANOCOBALAMIN; NIACINAMIDE; PYRIDOXINE HYDROCHLORIDE; RIBOFLAVIN 5'-PHOSPHATE SODIUM; SODIUM FLUORIDE; THIAMINE HYDROCHLORIDE; VITAMIN A PALMITATE
Strength Number 5; 35; 400; 2; 8; .4; .6; .5; .5; 1500
Strength Unit [iU]/mL; mg/mL; [iU]/mL; ug/mL; mg/mL; mg/mL; mg/mL; mg/mL; mg/mL; [iU]/mL
Pharmaceutical Classes Vitamin A [Chemical/Ingredient],Vitamin A [EPC],Nicotinic Acid [EPC],Nicotinic Acids [Chemical/Ingredient],Vitamin B 12 [Chemical/Ingredient],Vitamin B12 [EPC]

Complete Information of Multi Vitamin and Fluoride


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