Home
>
National Drug Code (NDC)
>
Dovonex
Dovonex - 50222-260-99 - (Calcipotriene)
Drug Information of Dovonex
| 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) |
Labeler Information of Dovonex
| 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 Information of Dovonex
| Package NDC: | 50222-260-99 |
| Package Description: | 25 CARTON in 1 CASE (50222-260-99) > 10 TUBE in 1 CARTON > 3 g in 1 TUBE |
NDC Information of Dovonex
| NDC Code | 50222-260-99 |
| Proprietary Name | Dovonex |
| Package Description | 25 CARTON in 1 CASE (50222-260-99) > 10 TUBE in 1 CARTON > 3 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] |
