 
                        | Product NDC: | 0603-7805 | 
| Proprietary Name: | Miconazole Nitrate | 
| Non Proprietary Name: | miconazole nitrate | 
| Active Ingredient(s): | 20 mg/g & nbsp; miconazole nitrate | 
| Administration Route(s): | TOPICAL | 
| Dosage Form(s): | CREAM | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 0603-7805 | 
| Labeler Name: | Qualitest Pharmaceuticals | 
| Product Type: | HUMAN OTC DRUG | 
| FDA Application Number: | part333C | 
| Marketing Category: | OTC MONOGRAPH FINAL | 
| Start Marketing Date: | 20030901 | 
| Package NDC: | 0603-7805-50 | 
| Package Description: | 1 TUBE in 1 CARTON (0603-7805-50) > 28.4 g in 1 TUBE | 
| NDC Code | 0603-7805-50 | 
| Proprietary Name | Miconazole Nitrate | 
| Package Description | 1 TUBE in 1 CARTON (0603-7805-50) > 28.4 g in 1 TUBE | 
| Product NDC | 0603-7805 | 
| Product Type Name | HUMAN OTC DRUG | 
| Non Proprietary Name | miconazole nitrate | 
| Dosage Form Name | CREAM | 
| Route Name | TOPICAL | 
| Start Marketing Date | 20030901 | 
| Marketing Category Name | OTC MONOGRAPH FINAL | 
| Labeler Name | Qualitest Pharmaceuticals | 
| Substance Name | MICONAZOLE NITRATE | 
| Strength Number | 20 | 
| Strength Unit | mg/g | 
| Pharmaceutical Classes |