Product NDC: | 0062-1650 |
Proprietary Name: | Ertaczo |
Non Proprietary Name: | Sertaconazole Nitrate |
Active Ingredient(s): | 20 mg/g & nbsp; Sertaconazole Nitrate |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0062-1650 |
Labeler Name: | Ortho-McNeil Janssen Pharmaceuticals, Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA021385 |
Marketing Category: | NDA |
Start Marketing Date: | 20111017 |
Package NDC: | 0062-1650-03 |
Package Description: | 1 TUBE in 1 CARTON (0062-1650-03) > 30 g in 1 TUBE |
NDC Code | 0062-1650-03 |
Proprietary Name | Ertaczo |
Package Description | 1 TUBE in 1 CARTON (0062-1650-03) > 30 g in 1 TUBE |
Product NDC | 0062-1650 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Sertaconazole Nitrate |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20111017 |
Marketing Category Name | NDA |
Labeler Name | Ortho-McNeil Janssen Pharmaceuticals, Inc |
Substance Name | SERTACONAZOLE NITRATE |
Strength Number | 20 |
Strength Unit | mg/g |
Pharmaceutical Classes | Azole Antifungal [EPC],Azoles [Chemical/Ingredient] |