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: | 10337-359-07 |
Package Description: | 7 mL in 1 TUBE (10337-359-07) |
NDC Code | 10337-359-07 |
Proprietary Name | Oxistat |
Package Description | 7 mL in 1 TUBE (10337-359-07) |
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] |