Ludent - 44946-1016-3 - (Sodium Fluoride)

Alphabetical Index


Drug Information of Ludent

Product NDC: 44946-1016
Proprietary Name: Ludent
Non Proprietary Name: Sodium Fluoride
Active Ingredient(s): .5    mg/1 & nbsp;   Sodium Fluoride
Administration Route(s): ORAL
Dosage Form(s): TABLET, CHEWABLE
Coding System: National Drug Codes(NDC)

Labeler Information of Ludent

Product NDC: 44946-1016
Labeler Name: Sancilio & Company Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20090910

Package Information of Ludent

Package NDC: 44946-1016-3
Package Description: 120 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (44946-1016-3)

NDC Information of Ludent

NDC Code 44946-1016-3
Proprietary Name Ludent
Package Description 120 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (44946-1016-3)
Product NDC 44946-1016
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Sodium Fluoride
Dosage Form Name TABLET, CHEWABLE
Route Name ORAL
Start Marketing Date 20090910
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Sancilio & Company Inc
Substance Name SODIUM FLUORIDE
Strength Number .5
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Ludent


General Information