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Desenex
Desenex - 0067-0949-15 - (MICONAZOLE NITRATE)
Drug Information of Desenex
| Product NDC: | 0067-0949 |
| Proprietary Name: | Desenex |
| Non Proprietary Name: | MICONAZOLE NITRATE |
| Active Ingredient(s): | 2 g/100g & nbsp; MICONAZOLE NITRATE |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | POWDER |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Desenex
| Product NDC: | 0067-0949 |
| Labeler Name: | Novartis Consumer Health, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333C |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20090803 |
Package Information of Desenex
| Package NDC: | 0067-0949-15 |
| Package Description: | 43 g in 1 CONTAINER (0067-0949-15) |
NDC Information of Desenex
| NDC Code | 0067-0949-15 |
| Proprietary Name | Desenex |
| Package Description | 43 g in 1 CONTAINER (0067-0949-15) |
| Product NDC | 0067-0949 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | MICONAZOLE NITRATE |
| Dosage Form Name | POWDER |
| Route Name | TOPICAL |
| Start Marketing Date | 20090803 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Novartis Consumer Health, Inc. |
| Substance Name | MICONAZOLE NITRATE |
| Strength Number | 2 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |
