| Product NDC: | 0288-2203 |
| Proprietary Name: | FLUORITAB CHEWABLE |
| Non Proprietary Name: | SODIUM FLUORIDE |
| Active Ingredient(s): | 1 mg/1 & nbsp; SODIUM FLUORIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, CHEWABLE |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 0288-2203 |
| Labeler Name: | Fluoritab Corporation |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20110109 |
| Package NDC: | 0288-2203-01 |
| Package Description: | 100 TABLET, CHEWABLE in 1 BOTTLE (0288-2203-01) |
| NDC Code | 0288-2203-01 |
| Proprietary Name | FLUORITAB CHEWABLE |
| Package Description | 100 TABLET, CHEWABLE in 1 BOTTLE (0288-2203-01) |
| Product NDC | 0288-2203 |
| 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 | 1 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |