 
                        | Product NDC: | 0904-5415 | 
| Proprietary Name: | Miconazole 3 Combination Pack | 
| Non Proprietary Name: | miconazole nitrate | 
| Active Ingredient(s): | & nbsp; miconazole nitrate | 
| Administration Route(s): | VAGINAL | 
| Dosage Form(s): | KIT | 
| Coding System: | National Drug Codes(NDC) | 
| Product NDC: | 0904-5415 | 
| Labeler Name: | Major Pharmaceuticals | 
| Product Type: | HUMAN OTC DRUG | 
| FDA Application Number: | ANDA074926 | 
| Marketing Category: | ANDA | 
| Start Marketing Date: | 20021202 | 
| Package NDC: | 0904-5415-01 | 
| Package Description: | 1 KIT in 1 PACKAGE, COMBINATION (0904-5415-01) * 3 SUPPOSITORY in 1 BLISTER PACK * 9 g in 1 TUBE | 
| NDC Code | 0904-5415-01 | 
| Proprietary Name | Miconazole 3 Combination Pack | 
| Package Description | 1 KIT in 1 PACKAGE, COMBINATION (0904-5415-01) * 3 SUPPOSITORY in 1 BLISTER PACK * 9 g in 1 TUBE | 
| Product NDC | 0904-5415 | 
| Product Type Name | HUMAN OTC DRUG | 
| Non Proprietary Name | miconazole nitrate | 
| Dosage Form Name | KIT | 
| Route Name | VAGINAL | 
| Start Marketing Date | 20021202 | 
| Marketing Category Name | ANDA | 
| Labeler Name | Major Pharmaceuticals | 
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