Product NDC: | 11673-199 |
Proprietary Name: | up and up miconazole |
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: | 11673-199 |
Labeler Name: | Target Corporation |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | ANDA079114 |
Marketing Category: | ANDA |
Start Marketing Date: | 20100708 |
Package NDC: | 11673-199-00 |
Package Description: | 1 KIT in 1 CARTON (11673-199-00) * 1 BLISTER PACK in 1 KIT > 1 INSERT in 1 BLISTER PACK * 1 TUBE in 1 KIT > 9 g in 1 TUBE |
NDC Code | 11673-199-00 |
Proprietary Name | up and up miconazole |
Package Description | 1 KIT in 1 CARTON (11673-199-00) * 1 BLISTER PACK in 1 KIT > 1 INSERT in 1 BLISTER PACK * 1 TUBE in 1 KIT > 9 g in 1 TUBE |
Product NDC | 11673-199 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Miconazole nitrate |
Dosage Form Name | KIT |
Route Name | |
Start Marketing Date | 20100708 |
Marketing Category Name | ANDA |
Labeler Name | Target Corporation |
Substance Name | |
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