Product NDC: | 63736-026 |
Proprietary Name: | Monistat 7 |
Non Proprietary Name: | Miconazole Nitrate |
Active Ingredient(s): | 20 mg/g & nbsp; Miconazole Nitrate |
Administration Route(s): | VAGINAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 63736-026 |
Labeler Name: | Insight Pharmaceuticals |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | NDA017450 |
Marketing Category: | NDA |
Start Marketing Date: | 20100415 |
Package NDC: | 63736-026-15 |
Package Description: | 7 TUBE, WITH APPLICATOR in 1 CARTON (63736-026-15) > 45 g in 1 TUBE, WITH APPLICATOR |
NDC Code | 63736-026-15 |
Proprietary Name | Monistat 7 |
Package Description | 7 TUBE, WITH APPLICATOR in 1 CARTON (63736-026-15) > 45 g in 1 TUBE, WITH APPLICATOR |
Product NDC | 63736-026 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Miconazole Nitrate |
Dosage Form Name | CREAM |
Route Name | VAGINAL |
Start Marketing Date | 20100415 |
Marketing Category Name | NDA |
Labeler Name | Insight Pharmaceuticals |
Substance Name | MICONAZOLE NITRATE |
Strength Number | 20 |
Strength Unit | mg/g |
Pharmaceutical Classes |