Product NDC: | 21695-854 |
Proprietary Name: | Miconazole Nitrate |
Non Proprietary Name: | Miconazole Nitrate |
Active Ingredient(s): | 20 mg/g & nbsp; Miconazole Nitrate |
Administration Route(s): | VAGINAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 21695-854 |
Labeler Name: | Rebel Distributors Corp |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | part333C |
Marketing Category: | OTC MONOGRAPH FINAL |
Start Marketing Date: | 20080101 |
Package NDC: | 21695-854-45 |
Package Description: | 45 g in 1 TUBE (21695-854-45) |
NDC Code | 21695-854-45 |
Proprietary Name | Miconazole Nitrate |
Package Description | 45 g in 1 TUBE (21695-854-45) |
Product NDC | 21695-854 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | Miconazole Nitrate |
Dosage Form Name | CREAM |
Route Name | VAGINAL |
Start Marketing Date | 20080101 |
Marketing Category Name | OTC MONOGRAPH FINAL |
Labeler Name | Rebel Distributors Corp |
Substance Name | MICONAZOLE NITRATE |
Strength Number | 20 |
Strength Unit | mg/g |
Pharmaceutical Classes |