| 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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