Product NDC: | 0145-0002 |
Proprietary Name: | VUSION |
Non Proprietary Name: | miconazole nitrate, zinc oxide, white petrolatum |
Active Ingredient(s): | 2.5; 813.5; 150 mg/g; mg/g; mg/g & nbsp; miconazole nitrate, zinc oxide, white petrolatum |
Administration Route(s): | TOPICAL |
Dosage Form(s): | OINTMENT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0145-0002 |
Labeler Name: | Stiefel Laboratories Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA021026 |
Marketing Category: | NDA |
Start Marketing Date: | 20070514 |
Package NDC: | 0145-0002-04 |
Package Description: | 1 TUBE in 1 CARTON (0145-0002-04) > 50 g in 1 TUBE |
NDC Code | 0145-0002-04 |
Proprietary Name | VUSION |
Package Description | 1 TUBE in 1 CARTON (0145-0002-04) > 50 g in 1 TUBE |
Product NDC | 0145-0002 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | miconazole nitrate, zinc oxide, white petrolatum |
Dosage Form Name | OINTMENT |
Route Name | TOPICAL |
Start Marketing Date | 20070514 |
Marketing Category Name | NDA |
Labeler Name | Stiefel Laboratories Inc |
Substance Name | MICONAZOLE NITRATE; PETROLATUM; ZINC OXIDE |
Strength Number | 2.5; 813.5; 150 |
Strength Unit | mg/g; mg/g; mg/g |
Pharmaceutical Classes | Azole Antifungal [EPC],Azoles [Chemical/Ingredient] |