Home
>
National Drug Code (NDC)
>
Conazol
Conazol - 75940-121-30 - (Miconazole Nitrate)
Drug Information of Conazol
| Product NDC: | 75940-121 |
| Proprietary Name: | Conazol |
| Non Proprietary Name: | Miconazole Nitrate |
| Active Ingredient(s): | 20 mg/g & nbsp; Miconazole Nitrate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Conazol
| Product NDC: | 75940-121 |
| Labeler Name: | MarcasUSA LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333C |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20110419 |
Package Information of Conazol
| Package NDC: | 75940-121-30 |
| Package Description: | 30 g in 1 TUBE (75940-121-30) |
NDC Information of Conazol
| NDC Code | 75940-121-30 |
| Proprietary Name | Conazol |
| Package Description | 30 g in 1 TUBE (75940-121-30) |
| Product NDC | 75940-121 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Miconazole Nitrate |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20110419 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | MarcasUSA LLC |
| Substance Name | MICONAZOLE NITRATE |
| Strength Number | 20 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
