 
                        | Product NDC: | 0363-0737 | 
| Proprietary Name: | Miconazole 1 | 
| 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: | 0363-0737 | 
| Labeler Name: | Walgreen Company | 
| Product Type: | HUMAN OTC DRUG | 
| FDA Application Number: | ANDA079114 | 
| Marketing Category: | ANDA | 
| Start Marketing Date: | 20100608 | 
| Package NDC: | 0363-0737-45 | 
| Package Description: | 1 KIT in 1 CARTON (0363-0737-45) * 9 g in 1 TUBE * 1 SWAB in 1 PACKAGE * 1 INSERT in 1 BLISTER PACK | 
| NDC Code | 0363-0737-45 | 
| Proprietary Name | Miconazole 1 | 
| Package Description | 1 KIT in 1 CARTON (0363-0737-45) * 9 g in 1 TUBE * 1 SWAB in 1 PACKAGE * 1 INSERT in 1 BLISTER PACK | 
| Product NDC | 0363-0737 | 
| Product Type Name | HUMAN OTC DRUG | 
| Non Proprietary Name | Miconazole nitrate | 
| Dosage Form Name | KIT | 
| Route Name | |
| Start Marketing Date | 20100608 | 
| Marketing Category Name | ANDA | 
| Labeler Name | Walgreen Company | 
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |