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FLUORIDE DROPS
FLUORIDE DROPS - 0288-5523-01 - (SODIUM FLUORIDE)
Drug Information of FLUORIDE DROPS
| Product NDC: | 0288-5523 |
| Proprietary Name: | FLUORIDE DROPS |
| Non Proprietary Name: | SODIUM FLUORIDE |
| Active Ingredient(s): | 2.5 mg/mL & nbsp; SODIUM FLUORIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of FLUORIDE DROPS
| Product NDC: | 0288-5523 |
| Labeler Name: | Fluoritab Corporation |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20110109 |
Package Information of FLUORIDE DROPS
| Package NDC: | 0288-5523-01 |
| Package Description: | 30 mL in 1 BOTTLE, DROPPER (0288-5523-01) |
NDC Information of FLUORIDE DROPS
| NDC Code | 0288-5523-01 |
| Proprietary Name | FLUORIDE DROPS |
| Package Description | 30 mL in 1 BOTTLE, DROPPER (0288-5523-01) |
| Product NDC | 0288-5523 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | SODIUM FLUORIDE |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20110109 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Fluoritab Corporation |
| Substance Name | SODIUM FLUORIDE |
| Strength Number | 2.5 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |
