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DentaGel
DentaGel - 64980-307-60 - (Sodium fluoride)
Drug Information of DentaGel
| Product NDC: | 64980-307 |
| Proprietary Name: | DentaGel |
| Non Proprietary Name: | Sodium fluoride |
| Active Ingredient(s): | 1.1 g/100g & nbsp; Sodium fluoride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | GEL |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of DentaGel
| Product NDC: | 64980-307 |
| Labeler Name: | Rising Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20120501 |
Package Information of DentaGel
| Package NDC: | 64980-307-60 |
| Package Description: | 56 g in 1 TUBE (64980-307-60) |
NDC Information of DentaGel
| NDC Code | 64980-307-60 |
| Proprietary Name | DentaGel |
| Package Description | 56 g in 1 TUBE (64980-307-60) |
| Product NDC | 64980-307 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Sodium fluoride |
| Dosage Form Name | GEL |
| Route Name | ORAL |
| Start Marketing Date | 20120501 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Rising Pharmaceuticals, Inc. |
| Substance Name | SODIUM FLUORIDE |
| Strength Number | 1.1 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |
