Product NDC: | 0603-7805 |
Proprietary Name: | Miconazole Nitrate |
Non Proprietary Name: | miconazole nitrate |
Active Ingredient(s): | 20 mg/g & nbsp; miconazole nitrate |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0603-7805 |
Labeler Name: | Qualitest Pharmaceuticals |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333C |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20030901 |
Package NDC: | 0603-7805-50 |
Package Description: | 1 TUBE in 1 CARTON (0603-7805-50) > 28.4 g in 1 TUBE |
NDC Code | 0603-7805-50 |
Proprietary Name | Miconazole Nitrate |
Package Description | 1 TUBE in 1 CARTON (0603-7805-50) > 28.4 g in 1 TUBE |
Product NDC | 0603-7805 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | miconazole nitrate |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20030901 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Qualitest Pharmaceuticals |
Substance Name | MICONAZOLE NITRATE |
Strength Number | 20 |
Strength Unit | mg/g |
Pharmaceutical Classes |