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Oxistat
Oxistat - 21695-459-30 - (oxiconazole nitrate)
Drug Information of Oxistat
| Product NDC: | 21695-459 |
| Proprietary Name: | Oxistat |
| Non Proprietary Name: | oxiconazole nitrate |
| Active Ingredient(s): | 30 mg/g & nbsp; oxiconazole nitrate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | LOTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Oxistat
| Product NDC: | 21695-459 |
| Labeler Name: | Rebel Distributors Corp. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020209 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20060125 |
Package Information of Oxistat
| Package NDC: | 21695-459-30 |
| Package Description: | 30 g in 1 TUBE (21695-459-30) |
NDC Information of Oxistat
| NDC Code | 21695-459-30 |
| Proprietary Name | Oxistat |
| Package Description | 30 g in 1 TUBE (21695-459-30) |
| Product NDC | 21695-459 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | oxiconazole nitrate |
| Dosage Form Name | LOTION |
| Route Name | TOPICAL |
| Start Marketing Date | 20060125 |
| Marketing Category Name | NDA |
| Labeler Name | Rebel Distributors Corp. |
| Substance Name | OXICONAZOLE NITRATE |
| Strength Number | 30 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | Azole Antifungal [EPC],Azoles [Chemical/Ingredient] |
