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GenRx Daily Defense Antifungal
GenRx Daily Defense Antifungal - 59088-924-07 - (Miconazole Nitrate)
Drug Information of GenRx Daily Defense Antifungal
| Product NDC: | 59088-924 |
| Proprietary Name: | GenRx Daily Defense Antifungal |
| Non Proprietary Name: | Miconazole Nitrate |
| Active Ingredient(s): | 20 mg/g & nbsp; Miconazole Nitrate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | POWDER |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of GenRx Daily Defense Antifungal
| Product NDC: | 59088-924 |
| Labeler Name: | PureTek Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333C |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20130108 |
Package Information of GenRx Daily Defense Antifungal
| Package NDC: | 59088-924-07 |
| Package Description: | 85 g in 1 BOTTLE, PLASTIC (59088-924-07) |
NDC Information of GenRx Daily Defense Antifungal
| NDC Code | 59088-924-07 |
| Proprietary Name | GenRx Daily Defense Antifungal |
| Package Description | 85 g in 1 BOTTLE, PLASTIC (59088-924-07) |
| Product NDC | 59088-924 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Miconazole Nitrate |
| Dosage Form Name | POWDER |
| Route Name | TOPICAL |
| Start Marketing Date | 20130108 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | PureTek Corporation |
| Substance Name | MICONAZOLE NITRATE |
| Strength Number | 20 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
