| Product NDC: | 42254-319 |
| 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: | 42254-319 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333C |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20030901 |
| Package NDC: | 42254-319-30 |
| Package Description: | 1 TUBE in 1 CARTON (42254-319-30) > 28.4 g in 1 TUBE |
| NDC Code | 42254-319-30 |
| Proprietary Name | Miconazole Nitrate |
| Package Description | 1 TUBE in 1 CARTON (42254-319-30) > 28.4 g in 1 TUBE |
| Product NDC | 42254-319 |
| 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 | Rebel Distributors Corp |
| Substance Name | MICONAZOLE NITRATE |
| Strength Number | 20 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |