 
                        | Product NDC: | 63868-198 | 
| Proprietary Name: | Miconazole 7 | 
| Non Proprietary Name: | Miconazole Nitrate | 
| Active Ingredient(s): | 2 g/100g & nbsp; Miconazole Nitrate | 
| Administration Route(s): | VAGINAL | 
| Dosage Form(s): | CREAM | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 63868-198 | 
| Labeler Name: | CDMA/Quality Choice | 
| Product Type: | HUMAN OTC DRUG | 
| FDA Application Number: | ANDA074164 | 
| Marketing Category: | ANDA | 
| Start Marketing Date: | 20100701 | 
| Package NDC: | 63868-198-45 | 
| Package Description: | 1 TUBE, WITH APPLICATOR in 1 CARTON (63868-198-45) > 45 g in 1 TUBE, WITH APPLICATOR | 
| NDC Code | 63868-198-45 | 
| Proprietary Name | Miconazole 7 | 
| Package Description | 1 TUBE, WITH APPLICATOR in 1 CARTON (63868-198-45) > 45 g in 1 TUBE, WITH APPLICATOR | 
| Product NDC | 63868-198 | 
| Product Type Name | HUMAN OTC DRUG | 
| Non Proprietary Name | Miconazole Nitrate | 
| Dosage Form Name | CREAM | 
| Route Name | VAGINAL | 
| Start Marketing Date | 20100701 | 
| Marketing Category Name | ANDA | 
| Labeler Name | CDMA/Quality Choice | 
| Substance Name | MICONAZOLE NITRATE | 
| Strength Number | 2 | 
| Strength Unit | g/100g | 
| Pharmaceutical Classes |