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Kendall Antifungal
Kendall Antifungal - 28851-692-01 - (Miconazole nitrate)
Drug Information of Kendall Antifungal
| Product NDC: | 28851-692 |
| Proprietary Name: | Kendall Antifungal |
| Non Proprietary Name: | Miconazole nitrate |
| Active Ingredient(s): | 2 g/100g & nbsp; Miconazole nitrate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Kendall Antifungal
| Product NDC: | 28851-692 |
| Labeler Name: | Covidien Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333C |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110414 |
Package Information of Kendall Antifungal
| Package NDC: | 28851-692-01 |
| Package Description: | 118 g in 1 TUBE (28851-692-01) |
NDC Information of Kendall Antifungal
| NDC Code | 28851-692-01 |
| Proprietary Name | Kendall Antifungal |
| Package Description | 118 g in 1 TUBE (28851-692-01) |
| Product NDC | 28851-692 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Miconazole nitrate |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20110414 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Covidien Inc. |
| Substance Name | MICONAZOLE NITRATE |
| Strength Number | 2 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |
