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Ludent
Ludent - 44946-1009-3 - (Sodium Fluoride)
Drug Information of Ludent
| Product NDC: | 44946-1009 |
| Proprietary Name: | Ludent |
| 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) |
Labeler Information of Ludent
| Product NDC: | 44946-1009 |
| Labeler Name: | Sancilio & Company Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20111220 |
Package Information of Ludent
| Package NDC: | 44946-1009-3 |
| Package Description: | 24 BOTTLE in 1 BOX (44946-1009-3) > 120 TABLET, CHEWABLE in 1 BOTTLE |
NDC Information of Ludent
| NDC Code | 44946-1009-3 |
| Proprietary Name | Ludent |
| Package Description | 24 BOTTLE in 1 BOX (44946-1009-3) > 120 TABLET, CHEWABLE in 1 BOTTLE |
| Product NDC | 44946-1009 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Sodium Fluoride |
| Dosage Form Name | TABLET, CHEWABLE |
| Route Name | ORAL |
| Start Marketing Date | 20111220 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Sancilio & Company Inc |
| Substance Name | SODIUM FLUORIDE |
| Strength Number | .5 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
