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Fluoride
Fluoride - 51862-172-12 - (Fluoride)
Drug Information of Fluoride
| Product NDC: | 51862-172 |
| Proprietary Name: | Fluoride |
| Non Proprietary Name: | Fluoride |
| Active Ingredient(s): | 1 mg/1 & nbsp; Fluoride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, CHEWABLE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Fluoride
| Product NDC: | 51862-172 |
| 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 Fluoride
| Package NDC: | 51862-172-12 |
| Package Description: | 120 TABLET, CHEWABLE in 1 BOTTLE (51862-172-12) |
NDC Information of Fluoride
| NDC Code | 51862-172-12 |
| Proprietary Name | Fluoride |
| Package Description | 120 TABLET, CHEWABLE in 1 BOTTLE (51862-172-12) |
| Product NDC | 51862-172 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Fluoride |
| Dosage Form Name | TABLET, CHEWABLE |
| Route Name | ORAL |
| Start Marketing Date | 20110521 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Libertas Pharma, Inc. |
| Substance Name | SODIUM FLUORIDE |
| Strength Number | 1 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
