Product NDC: | 50222-260 |
Proprietary Name: | Dovonex |
Non Proprietary Name: | Calcipotriene |
Active Ingredient(s): | 50 ug/g & nbsp; Calcipotriene |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 50222-260 |
Labeler Name: | LEO Pharma Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA020554 |
Marketing Category: | NDA |
Start Marketing Date: | 19961001 |
Package NDC: | 50222-260-06 |
Package Description: | 100 CARTON in 1 CASE (50222-260-06) > 1 TUBE in 1 CARTON > 60 g in 1 TUBE |
NDC Code | 50222-260-06 |
Proprietary Name | Dovonex |
Package Description | 100 CARTON in 1 CASE (50222-260-06) > 1 TUBE in 1 CARTON > 60 g in 1 TUBE |
Product NDC | 50222-260 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Calcipotriene |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 19961001 |
Marketing Category Name | NDA |
Labeler Name | LEO Pharma Inc. |
Substance Name | CALCIPOTRIENE |
Strength Number | 50 |
Strength Unit | ug/g |
Pharmaceutical Classes | Vitamin D [Chemical/Ingredient],Vitamin D Analog [EPC] |