| Product NDC: | 63736-410 |
| Proprietary Name: | Tioconazole |
| Non Proprietary Name: | Tioconazole |
| Active Ingredient(s): | 300 mg/g & nbsp; Tioconazole |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 63736-410 |
| Labeler Name: | Insight Pharmaceuticals LLC |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA075915 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20011121 |
| Package NDC: | 63736-410-01 |
| Package Description: | 1 POUCH in 1 CARTON (63736-410-01) > 1 APPLICATOR in 1 POUCH > 4.6 g in 1 APPLICATOR |
| NDC Code | 63736-410-01 |
| Proprietary Name | Tioconazole |
| Package Description | 1 POUCH in 1 CARTON (63736-410-01) > 1 APPLICATOR in 1 POUCH > 4.6 g in 1 APPLICATOR |
| Product NDC | 63736-410 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Tioconazole |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 20011121 |
| Marketing Category Name | ANDA |
| Labeler Name | Insight Pharmaceuticals LLC |
| Substance Name | TIOCONAZOLE |
| Strength Number | 300 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |