| Product NDC: | 68788-9848 |
| Proprietary Name: | Econazole Nitrate |
| Non Proprietary Name: | Econazole Nitrate |
| Active Ingredient(s): | 10 mg/g & nbsp; Econazole Nitrate |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 68788-9848 |
| Labeler Name: | Preferred Pharmaceuticals, Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA076005 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120329 |
| Package NDC: | 68788-9848-3 |
| Package Description: | 30 g in 1 TUBE (68788-9848-3) |
| NDC Code | 68788-9848-3 |
| Proprietary Name | Econazole Nitrate |
| Package Description | 30 g in 1 TUBE (68788-9848-3) |
| Product NDC | 68788-9848 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Econazole Nitrate |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20120329 |
| Marketing Category Name | ANDA |
| Labeler Name | Preferred Pharmaceuticals, Inc |
| Substance Name | ECONAZOLE NITRATE |
| Strength Number | 10 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | Azole Antifungal [EPC],Azoles [Chemical/Ingredient] |