Product NDC: | 42254-319 |
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: | 42254-319 |
Labeler Name: | Rebel Distributors Corp |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333C |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20030901 |
Package NDC: | 42254-319-30 |
Package Description: | 1 TUBE in 1 CARTON (42254-319-30) > 28.4 g in 1 TUBE |
NDC Code | 42254-319-30 |
Proprietary Name | Miconazole Nitrate |
Package Description | 1 TUBE in 1 CARTON (42254-319-30) > 28.4 g in 1 TUBE |
Product NDC | 42254-319 |
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 | Rebel Distributors Corp |
Substance Name | MICONAZOLE NITRATE |
Strength Number | 20 |
Strength Unit | mg/g |
Pharmaceutical Classes |