Product NDC: | 11673-825 |
Proprietary Name: | up and up miconazole 7 |
Non Proprietary Name: | Miconazole nitrate |
Active Ingredient(s): | 2 g/100g & nbsp; Miconazole nitrate |
Administration Route(s): | VAGINAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 11673-825 |
Labeler Name: | Target Corporation |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | ANDA074760 |
Marketing Category: | ANDA |
Start Marketing Date: | 20090826 |
Package NDC: | 11673-825-29 |
Package Description: | 1 TUBE in 1 CARTON (11673-825-29) > 45 g in 1 TUBE |
NDC Code | 11673-825-29 |
Proprietary Name | up and up miconazole 7 |
Package Description | 1 TUBE in 1 CARTON (11673-825-29) > 45 g in 1 TUBE |
Product NDC | 11673-825 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Miconazole nitrate |
Dosage Form Name | CREAM |
Route Name | VAGINAL |
Start Marketing Date | 20090826 |
Marketing Category Name | ANDA |
Labeler Name | Target Corporation |
Substance Name | MICONAZOLE NITRATE |
Strength Number | 2 |
Strength Unit | g/100g |
Pharmaceutical Classes |