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Antifungal
Antifungal - 68345-817-25 - (Miconazole Nitrate)
Drug Information of Antifungal
| Product NDC: | 68345-817 |
| Proprietary Name: | Antifungal |
| 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 Antifungal
| Product NDC: | 68345-817 |
| Labeler Name: | PSS World Medical, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333C |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20120905 |
Package Information of Antifungal
| Package NDC: | 68345-817-25 |
| Package Description: | 142 g in 1 TUBE (68345-817-25) |
NDC Information of Antifungal
| NDC Code | 68345-817-25 |
| Proprietary Name | Antifungal |
| Package Description | 142 g in 1 TUBE (68345-817-25) |
| Product NDC | 68345-817 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Miconazole Nitrate |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20120905 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | PSS World Medical, Inc. |
| Substance Name | MICONAZOLE NITRATE |
| Strength Number | 20 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
