| Product NDC: | 49348-355 |
| Proprietary Name: | sunmark miconazole 3 |
| 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: | 49348-355 |
| Labeler Name: | McKesson |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | ANDA075329 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20030905 |
| Package NDC: | 49348-355-43 |
| Package Description: | 1 KIT in 1 CARTON (49348-355-43) * 3 SUPPOSITORY in 1 BLISTER PACK * 9 g in 1 TUBE |
| NDC Code | 49348-355-43 |
| Proprietary Name | sunmark miconazole 3 |
| Package Description | 1 KIT in 1 CARTON (49348-355-43) * 3 SUPPOSITORY in 1 BLISTER PACK * 9 g in 1 TUBE |
| Product NDC | 49348-355 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Miconazole nitrate |
| Dosage Form Name | KIT |
| Route Name | |
| Start Marketing Date | 20030905 |
| Marketing Category Name | ANDA |
| Labeler Name | McKesson |
| Substance Name | |
| Strength Number | |
| Strength Unit | |
| Pharmaceutical Classes |