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 |