Product NDC: | 44946-1015 |
Proprietary Name: | Ludent |
Non Proprietary Name: | Sodium Fluoride |
Active Ingredient(s): | .25 mg/1 & nbsp; Sodium Fluoride |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET, CHEWABLE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 44946-1015 |
Labeler Name: | Sancilio & Company Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20090910 |
Package NDC: | 44946-1015-2 |
Package Description: | 60 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (44946-1015-2) |
NDC Code | 44946-1015-2 |
Proprietary Name | Ludent |
Package Description | 60 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (44946-1015-2) |
Product NDC | 44946-1015 |
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 | .25 |
Strength Unit | mg/1 |
Pharmaceutical Classes |