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Micatin
Micatin - 65197-103-05 - (Miconazole nitrate)
Drug Information of Micatin
| Product NDC: | 65197-103 |
| Proprietary Name: | Micatin |
| 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) |
Labeler Information of Micatin
| Product NDC: | 65197-103 |
| Labeler Name: | WellSpring Pharmaceutical Corporation |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | part333C |
| Marketing Category: | OTC MONOGRAPH FINAL |
| Start Marketing Date: | 20090624 |
Package Information of Micatin
| Package NDC: | 65197-103-05 |
| Package Description: | 14 g in 1 TUBE (65197-103-05) |
NDC Information of Micatin
| NDC Code | 65197-103-05 |
| Proprietary Name | Micatin |
| Package Description | 14 g in 1 TUBE (65197-103-05) |
| Product NDC | 65197-103 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Miconazole nitrate |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20090624 |
| Marketing Category Name | OTC MONOGRAPH FINAL |
| Labeler Name | WellSpring Pharmaceutical Corporation |
| Substance Name | MICONAZOLE NITRATE |
| Strength Number | 20 |
| Strength Unit | mg/g |
| Pharmaceutical Classes |
