Home
>
National Drug Code (NDC)
>
Epiflur
Epiflur - 42806-060-10 - (Sodium Fluoride)
Drug Information of Epiflur
| Product NDC: | 42806-060 |
| Proprietary Name: | Epiflur |
| Non Proprietary Name: | Sodium Fluoride |
| Active Ingredient(s): | 1.1 mg/1 & nbsp; Sodium Fluoride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Epiflur
| Product NDC: | 42806-060 |
| Labeler Name: | Epic Pharma, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED DRUG OTHER |
| Start Marketing Date: | 20091019 |
Package Information of Epiflur
| Package NDC: | 42806-060-10 |
| Package Description: | 1000 TABLET in 1 BOTTLE (42806-060-10) |
NDC Information of Epiflur
| NDC Code | 42806-060-10 |
| Proprietary Name | Epiflur |
| Package Description | 1000 TABLET in 1 BOTTLE (42806-060-10) |
| Product NDC | 42806-060 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Sodium Fluoride |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20091019 |
| Marketing Category Name | UNAPPROVED DRUG OTHER |
| Labeler Name | Epic Pharma, LLC |
| Substance Name | SODIUM FLUORIDE |
| Strength Number | 1.1 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes |
