Product NDC: | 0288-1106 |
Proprietary Name: | FLUORITAB CHEWABLE |
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) |
Product NDC: | 0288-1106 |
Labeler Name: | Fluoritab Corporation |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20110109 |
Package NDC: | 0288-1106-02 |
Package Description: | 5000 TABLET, CHEWABLE in 1 BOTTLE (0288-1106-02) |
NDC Code | 0288-1106-02 |
Proprietary Name | FLUORITAB CHEWABLE |
Package Description | 5000 TABLET, CHEWABLE in 1 BOTTLE (0288-1106-02) |
Product NDC | 0288-1106 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | SODIUM FLUORIDE |
Dosage Form Name | TABLET, CHEWABLE |
Route Name | ORAL |
Start Marketing Date | 20110109 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | Fluoritab Corporation |
Substance Name | SODIUM FLUORIDE |
Strength Number | .5 |
Strength Unit | mg/1 |
Pharmaceutical Classes |