Fluoride - 51862-171-12 - (Fluoride)

Alphabetical Index


Drug Information of Fluoride

Product NDC: 51862-171
Proprietary Name: Fluoride
Non Proprietary Name: Fluoride
Active Ingredient(s): .5    mg/1 & nbsp;   Fluoride
Administration Route(s): ORAL
Dosage Form(s): TABLET, CHEWABLE
Coding System: National Drug Codes(NDC)

Labeler Information of Fluoride

Product NDC: 51862-171
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 Fluoride

Package NDC: 51862-171-12
Package Description: 120 TABLET, CHEWABLE in 1 BOTTLE (51862-171-12)

NDC Information of Fluoride

NDC Code 51862-171-12
Proprietary Name Fluoride
Package Description 120 TABLET, CHEWABLE in 1 BOTTLE (51862-171-12)
Product NDC 51862-171
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Fluoride
Dosage Form Name TABLET, CHEWABLE
Route Name ORAL
Start Marketing Date 20110521
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Libertas Pharma, Inc.
Substance Name SODIUM FLUORIDE
Strength Number .5
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Fluoride


General Information