Product NDC: | 54868-5042 |
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: | 54868-5042 |
Labeler Name: | Physicians Total Care, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA076075 |
Marketing Category: | ANDA |
Start Marketing Date: | 20040519 |
Package NDC: | 54868-5042-0 |
Package Description: | 1 TUBE in 1 CARTON (54868-5042-0) > 30 g in 1 TUBE |
NDC Code | 54868-5042-0 |
Proprietary Name | Econazole Nitrate |
Package Description | 1 TUBE in 1 CARTON (54868-5042-0) > 30 g in 1 TUBE |
Product NDC | 54868-5042 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | econazole nitrate |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20040519 |
Marketing Category Name | ANDA |
Labeler Name | Physicians Total Care, Inc. |
Substance Name | ECONAZOLE NITRATE |
Strength Number | 10 |
Strength Unit | mg/g |
Pharmaceutical Classes | Azole Antifungal [EPC],Azoles [Chemical/Ingredient] |