| Product NDC: | 11673-982 |
| Proprietary Name: | Up and Up Miconazole 3 |
| Non Proprietary Name: | Miconazole nitrate |
| Active Ingredient(s): | & nbsp; Miconazole nitrate |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 11673-982 |
| Labeler Name: | Target Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA076357 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090812 |
| Package NDC: | 11673-982-00 |
| Package Description: | 1 KIT in 1 CARTON (11673-982-00) * 1 APPLICATOR in 1 POUCH > 5 g in 1 APPLICATOR * 1 TUBE in 1 CARTON > 9 g in 1 TUBE |
| NDC Code | 11673-982-00 |
| Proprietary Name | Up and Up Miconazole 3 |
| Package Description | 1 KIT in 1 CARTON (11673-982-00) * 1 APPLICATOR in 1 POUCH > 5 g in 1 APPLICATOR * 1 TUBE in 1 CARTON > 9 g in 1 TUBE |
| Product NDC | 11673-982 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Miconazole nitrate |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20090812 |
| Marketing Category Name | ANDA |
| Labeler Name | Target Corporation |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
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