Product NDC: | 10337-358 |
Proprietary Name: | Oxistat |
Non Proprietary Name: | oxiconazole nitrate |
Active Ingredient(s): | 10 mg/g & nbsp; oxiconazole nitrate |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 10337-358 |
Labeler Name: | PharmaDerm a division of Fougera Pharmaceuticals Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA019828 |
Marketing Category: | NDA |
Start Marketing Date: | 19881230 |
Package NDC: | 10337-358-60 |
Package Description: | 1 TUBE in 1 CARTON (10337-358-60) > 60 g in 1 TUBE |
NDC Code | 10337-358-60 |
Proprietary Name | Oxistat |
Package Description | 1 TUBE in 1 CARTON (10337-358-60) > 60 g in 1 TUBE |
Product NDC | 10337-358 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | oxiconazole nitrate |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 19881230 |
Marketing Category Name | NDA |
Labeler Name | PharmaDerm a division of Fougera Pharmaceuticals Inc. |
Substance Name | OXICONAZOLE NITRATE |
Strength Number | 10 |
Strength Unit | mg/g |
Pharmaceutical Classes | Azole Antifungal [EPC],Azoles [Chemical/Ingredient] |