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Miconazole 7
Miconazole 7 - 68788-9772-4 - (Miconazole Nitrate)
Drug Information of Miconazole 7
| Product NDC: | 68788-9772 |
| Proprietary Name: | Miconazole 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) |
Labeler Information of Miconazole 7
| Product NDC: | 68788-9772 |
| Labeler Name: | Preferred Pharmaceuticals, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA074164 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20120727 |
Package Information of Miconazole 7
| Package NDC: | 68788-9772-4 |
| Package Description: | 1 TUBE, WITH APPLICATOR in 1 CARTON (68788-9772-4) > 45 g in 1 TUBE, WITH APPLICATOR |
NDC Information of Miconazole 7
| NDC Code | 68788-9772-4 |
| Proprietary Name | Miconazole 7 |
| Package Description | 1 TUBE, WITH APPLICATOR in 1 CARTON (68788-9772-4) > 45 g in 1 TUBE, WITH APPLICATOR |
| Product NDC | 68788-9772 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Miconazole Nitrate |
| Dosage Form Name | CREAM |
| Route Name | VAGINAL |
| Start Marketing Date | 20120727 |
| Marketing Category Name | ANDA |
| Labeler Name | Preferred Pharmaceuticals, Inc. |
| Substance Name | MICONAZOLE NITRATE |
| Strength Number | 20 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
