Product NDC: | 0430-3230 |
Proprietary Name: | TACLONEX |
Non Proprietary Name: | calcipotriene and betamethasone dipropionate |
Active Ingredient(s): | .643; 50 mg/g; ug/g & nbsp; calcipotriene and betamethasone dipropionate |
Administration Route(s): | TOPICAL |
Dosage Form(s): | OINTMENT |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0430-3230 |
Labeler Name: | Warner Chilcott (US), LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA021852 |
Marketing Category: | NDA |
Start Marketing Date: | 20080601 |
Package NDC: | 0430-3230-16 |
Package Description: | 50 CARTON in 1 CASE (0430-3230-16) > 1 TUBE in 1 CARTON > 100 g in 1 TUBE |
NDC Code | 0430-3230-16 |
Proprietary Name | TACLONEX |
Package Description | 50 CARTON in 1 CASE (0430-3230-16) > 1 TUBE in 1 CARTON > 100 g in 1 TUBE |
Product NDC | 0430-3230 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | calcipotriene and betamethasone dipropionate |
Dosage Form Name | OINTMENT |
Route Name | TOPICAL |
Start Marketing Date | 20080601 |
Marketing Category Name | NDA |
Labeler Name | Warner Chilcott (US), LLC |
Substance Name | BETAMETHASONE DIPROPIONATE; CALCIPOTRIENE |
Strength Number | .643; 50 |
Strength Unit | mg/g; ug/g |
Pharmaceutical Classes | Vitamin D [Chemical/Ingredient],Vitamin D Analog [EPC] |