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MICONAZOLE
MICONAZOLE - 61715-050-01 - (antifungal)
Drug Information of MICONAZOLE
| Product NDC: | 61715-050 |
| Proprietary Name: | MICONAZOLE |
| Non Proprietary Name: | antifungal |
| Active Ingredient(s): | 20 mg/g & nbsp; antifungal |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of MICONAZOLE
| Product NDC: | 61715-050 |
| Labeler Name: | Kinray, Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333C |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20130321 |
Package Information of MICONAZOLE
| Package NDC: | 61715-050-01 |
| Package Description: | 72 BOX in 1 CASE (61715-050-01) > 1 TUBE in 1 BOX > 28.4 g in 1 TUBE |
NDC Information of MICONAZOLE
| NDC Code | 61715-050-01 |
| Proprietary Name | MICONAZOLE |
| Package Description | 72 BOX in 1 CASE (61715-050-01) > 1 TUBE in 1 BOX > 28.4 g in 1 TUBE |
| Product NDC | 61715-050 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | antifungal |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20130321 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | Kinray, Inc. |
| Substance Name | MICONAZOLE NITRATE |
| Strength Number | 20 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
