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Tri-Vit with Fluoride Drops - 54569-1280-0 - (ascorbic acid and cholecalciferol and sodium fluoride and vitamin A palmitate)

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Drug Information of Tri-Vit with Fluoride Drops

Product NDC: 54569-1280
Proprietary Name: Tri-Vit with Fluoride Drops
Non Proprietary Name: ascorbic acid and cholecalciferol and sodium fluoride and vitamin A palmitate
Active Ingredient(s): 35; 400; .25; 1500    mg/mL; [iU]/mL; mg/mL; [iU]/mL & nbsp;   ascorbic acid and cholecalciferol and sodium fluoride and vitamin A palmitate
Administration Route(s): ORAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Tri-Vit with Fluoride Drops

Product NDC: 54569-1280
Labeler Name: A-S Medication Solutions LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 19950401

Package Information of Tri-Vit with Fluoride Drops

Package NDC: 54569-1280-0
Package Description: 1 BOTTLE, PLASTIC in 1 CARTON (54569-1280-0) > 50 mL in 1 BOTTLE, PLASTIC

NDC Information of Tri-Vit with Fluoride Drops

NDC Code 54569-1280-0
Proprietary Name Tri-Vit with Fluoride Drops
Package Description 1 BOTTLE, PLASTIC in 1 CARTON (54569-1280-0) > 50 mL in 1 BOTTLE, PLASTIC
Product NDC 54569-1280
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name ascorbic acid and cholecalciferol and sodium fluoride and vitamin A palmitate
Dosage Form Name SOLUTION
Route Name ORAL
Start Marketing Date 19950401
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name A-S Medication Solutions LLC
Substance Name ASCORBIC ACID; CHOLECALCIFEROL; SODIUM FLUORIDE; VITAMIN A PALMITATE
Strength Number 35; 400; .25; 1500
Strength Unit mg/mL; [iU]/mL; mg/mL; [iU]/mL
Pharmaceutical Classes Vitamin A [Chemical/Ingredient],Vitamin A [EPC],Vitamin D [Chemical/Ingredient],Vitamin D [EPC]

Complete Information of Tri-Vit with Fluoride Drops


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