Product NDC: | 44946-1050 |
Proprietary Name: | Neutral Sodium Fluoride |
Non Proprietary Name: | Sodium Fluoride |
Active Ingredient(s): | 20 mg/mL & nbsp; Sodium Fluoride |
Administration Route(s): | ORAL |
Dosage Form(s): | RINSE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 44946-1050 |
Labeler Name: | Sancilio & Company Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED DRUG OTHER |
Start Marketing Date: | 20130101 |
Package NDC: | 44946-1050-0 |
Package Description: | 473 mL in 1 BOTTLE, PLASTIC (44946-1050-0) |
NDC Code | 44946-1050-0 |
Proprietary Name | Neutral Sodium Fluoride |
Package Description | 473 mL in 1 BOTTLE, PLASTIC (44946-1050-0) |
Product NDC | 44946-1050 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Sodium Fluoride |
Dosage Form Name | RINSE |
Route Name | ORAL |
Start Marketing Date | 20130101 |
Marketing Category Name | UNAPPROVED DRUG OTHER |
Labeler Name | Sancilio & Company Inc |
Substance Name | SODIUM FLUORIDE |
Strength Number | 20 |
Strength Unit | mg/mL |
Pharmaceutical Classes |