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Alpha-Pro
Alpha-Pro - 55346-0943-1 - (Sodium Fluoride and Hydrofluoric Acid)
Drug Information of Alpha-Pro
| Product NDC: | 55346-0943 |
| Proprietary Name: | Alpha-Pro |
| Non Proprietary Name: | Sodium Fluoride and Hydrofluoric Acid |
| Active Ingredient(s): | 4.4; 7.9 mg/g; mg/g & nbsp; Sodium Fluoride and Hydrofluoric Acid |
| Administration Route(s): | DENTAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Alpha-Pro
| Product NDC: | 55346-0943 |
| Labeler Name: | Dental Technologies, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20130401 |
Package Information of Alpha-Pro
| Package NDC: | 55346-0943-1 |
| Package Description: | 497 g in 1 BOTTLE (55346-0943-1) |
NDC Information of Alpha-Pro
| NDC Code | 55346-0943-1 |
| Proprietary Name | Alpha-Pro |
| Package Description | 497 g in 1 BOTTLE (55346-0943-1) |
| Product NDC | 55346-0943 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Sodium Fluoride and Hydrofluoric Acid |
| Dosage Form Name | GEL |
| Route Name | DENTAL |
| Start Marketing Date | 20130401 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Dental Technologies, Inc. |
| Substance Name | HYDROFLUORIC ACID; SODIUM FLUORIDE |
| Strength Number | 4.4; 7.9 |
| Strength Unit | mg/g; mg/g |
| Pharmaceutical Classes |
