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Sodium Fluoride
Sodium Fluoride - 51862-165-50 - (Sodium Fluoride)
Drug Information of Sodium Fluoride
| Product NDC: | 51862-165 |
| Proprietary Name: | Sodium Fluoride |
| Non Proprietary Name: | Sodium Fluoride |
| Active Ingredient(s): | .5 mg/mL & nbsp; Sodium Fluoride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SOLUTION/ DROPS |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Sodium Fluoride
| Product NDC: | 51862-165 |
| 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 Sodium Fluoride
| Package NDC: | 51862-165-50 |
| Package Description: | 1 BOTTLE in 1 CARTON (51862-165-50) > 50 mL in 1 BOTTLE |
NDC Information of Sodium Fluoride
| NDC Code | 51862-165-50 |
| Proprietary Name | Sodium Fluoride |
| Package Description | 1 BOTTLE in 1 CARTON (51862-165-50) > 50 mL in 1 BOTTLE |
| Product NDC | 51862-165 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Sodium Fluoride |
| Dosage Form Name | SOLUTION/ DROPS |
| 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/mL |
| Pharmaceutical Classes |
