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] |