| Product NDC: | 63736-003 |
| Proprietary Name: | Monistat 7 Combination Pack |
| Non Proprietary Name: | Miconazole Nitrate |
| Active Ingredient(s): | & nbsp; Miconazole Nitrate |
| Administration Route(s): | |
| Dosage Form(s): | KIT |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 63736-003 |
| Labeler Name: | Insight Pharmaceuticals |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | NDA017450 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19930426 |
| Package NDC: | 63736-003-07 |
| Package Description: | 1 KIT in 1 PACKAGE, COMBINATION (63736-003-07) * .1 g in 1 TUBE, WITH APPLICATOR * .009 g in 1 TUBE |
| NDC Code | 63736-003-07 |
| Proprietary Name | Monistat 7 Combination Pack |
| Package Description | 1 KIT in 1 PACKAGE, COMBINATION (63736-003-07) * .1 g in 1 TUBE, WITH APPLICATOR * .009 g in 1 TUBE |
| Product NDC | 63736-003 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Miconazole Nitrate |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 19930426 |
| Marketing Category Name | NDA |
| Labeler Name | Insight Pharmaceuticals |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |