| Product NDC: | 10337-359 |
| Proprietary Name: | Oxistat |
| Non Proprietary Name: | oxiconazole nitrate |
| Active Ingredient(s): | 10 mg/mL & nbsp; oxiconazole nitrate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 10337-359 |
| Labeler Name: | PharmaDerm a division of Fougera Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020209 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19920930 |
| Package NDC: | 10337-359-30 |
| Package Description: | 1 TUBE in 1 CARTON (10337-359-30) > 30 mL in 1 TUBE |
| NDC Code | 10337-359-30 |
| Proprietary Name | Oxistat |
| Package Description | 1 TUBE in 1 CARTON (10337-359-30) > 30 mL in 1 TUBE |
| Product NDC | 10337-359 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | oxiconazole nitrate |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 19920930 |
| Marketing Category Name | NDA |
| Labeler Name | PharmaDerm a division of Fougera Pharmaceuticals Inc. |
| Substance Name | OXICONAZOLE NITRATE |
| Strength Number | 10 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Azole Antifungal [EPC],Azoles [Chemical/Ingredient] |