| Product NDC: | 11673-426 |
| Proprietary Name: | Up and up tioconazole 1 |
| Non Proprietary Name: | Tioconazole |
| Active Ingredient(s): | 6.5 g/100g & nbsp; Tioconazole |
| Administration Route(s): | VAGINAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 11673-426 |
| Labeler Name: | Target Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA075915 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090708 |
| Package NDC: | 11673-426-54 |
| Package Description: | 1 POUCH in 1 CARTON (11673-426-54) > 1 APPLICATOR in 1 POUCH > 4.6 g in 1 APPLICATOR |
| NDC Code | 11673-426-54 |
| Proprietary Name | Up and up tioconazole 1 |
| Package Description | 1 POUCH in 1 CARTON (11673-426-54) > 1 APPLICATOR in 1 POUCH > 4.6 g in 1 APPLICATOR |
| Product NDC | 11673-426 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Tioconazole |
| Dosage Form Name | OINTMENT |
| Route Name | VAGINAL |
| Start Marketing Date | 20090708 |
| Marketing Category Name | ANDA |
| Labeler Name | Target Corporation |
| Substance Name | TIOCONAZOLE |
| Strength Number | 6.5 |
| Strength Unit | g/100g |
| Pharmaceutical Classes |