| Product NDC: | 63736-025 |
| 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: | 63736-025 |
| Labeler Name: | Insight Pharmaceuticals |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | NDA017450 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19930426 |
| Package NDC: | 63736-025-15 |
| Package Description: | 1 TUBE, WITH APPLICATOR in 1 CARTON (63736-025-15) > 45 g in 1 TUBE, WITH APPLICATOR |
| NDC Code | 63736-025-15 |
| Proprietary Name | Monistat 7 |
| Package Description | 1 TUBE, WITH APPLICATOR in 1 CARTON (63736-025-15) > 45 g in 1 TUBE, WITH APPLICATOR |
| Product NDC | 63736-025 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Miconazole Nitrate |
| Dosage Form Name | CREAM |
| Route Name | VAGINAL |
| Start Marketing Date | 19930426 |
| Marketing Category Name | NDA |
| Labeler Name | Insight Pharmaceuticals |
| Substance Name | MICONAZOLE NITRATE |
| Strength Number | 20 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |