Product NDC: | 68754-150 |
Proprietary Name: | Medicated Anti-Fungal Miconazole |
Non Proprietary Name: | Miconazole Nitrate |
Active Ingredient(s): | 2 g/100g & nbsp; Miconazole Nitrate |
Administration Route(s): | TOPICAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 68754-150 |
Labeler Name: | American Spraytech, LLC |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333 |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20100602 |
Package NDC: | 68754-150-00 |
Package Description: | 150 g in 1 CAN (68754-150-00) |
NDC Code | 68754-150-00 |
Proprietary Name | Medicated Anti-Fungal Miconazole |
Package Description | 150 g in 1 CAN (68754-150-00) |
Product NDC | 68754-150 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Miconazole Nitrate |
Dosage Form Name | LIQUID |
Route Name | TOPICAL |
Start Marketing Date | 20100602 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | American Spraytech, LLC |
Substance Name | MICONAZOLE NITRATE |
Strength Number | 2 |
Strength Unit | g/100g |
Pharmaceutical Classes |