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Ionite APF
Ionite APF - 53045-235-17 - (Sodium Fluoride)
Drug Information of Ionite APF
| Product NDC: | 53045-235 |
| Proprietary Name: | Ionite APF |
| Non Proprietary Name: | Sodium Fluoride |
| Active Ingredient(s): | 4.41 g/490g & nbsp; Sodium Fluoride |
| Administration Route(s): | DENTAL; ORAL; TOPICAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Ionite APF
| Product NDC: | 53045-235 |
| Labeler Name: | Dharma Research, inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20130101 |
Package Information of Ionite APF
| Package NDC: | 53045-235-17 |
| Package Description: | 490 g in 1 BOTTLE (53045-235-17) |
NDC Information of Ionite APF
| NDC Code | 53045-235-17 |
| Proprietary Name | Ionite APF |
| Package Description | 490 g in 1 BOTTLE (53045-235-17) |
| Product NDC | 53045-235 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Sodium Fluoride |
| Dosage Form Name | GEL |
| Route Name | DENTAL; ORAL; TOPICAL |
| Start Marketing Date | 20130101 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Dharma Research, inc. |
| Substance Name | SODIUM FLUORIDE |
| Strength Number | 4.41 |
| Strength Unit | g/490g |
| Pharmaceutical Classes |
