Product NDC: | 0781-7117 |
Proprietary Name: | Calcipotriene |
Non Proprietary Name: | Calcipotriene |
Active Ingredient(s): | .05 mg/g & nbsp; Calcipotriene |
Administration Route(s): | TOPICAL |
Dosage Form(s): | CREAM |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0781-7117 |
Labeler Name: | Sandoz Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA200935 |
Marketing Category: | ANDA |
Start Marketing Date: | 20120727 |
Package NDC: | 0781-7117-83 |
Package Description: | 1 TUBE in 1 CARTON (0781-7117-83) > 120 g in 1 TUBE |
NDC Code | 0781-7117-83 |
Proprietary Name | Calcipotriene |
Package Description | 1 TUBE in 1 CARTON (0781-7117-83) > 120 g in 1 TUBE |
Product NDC | 0781-7117 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Calcipotriene |
Dosage Form Name | CREAM |
Route Name | TOPICAL |
Start Marketing Date | 20120727 |
Marketing Category Name | ANDA |
Labeler Name | Sandoz Inc. |
Substance Name | CALCIPOTRIENE |
Strength Number | .05 |
Strength Unit | mg/g |
Pharmaceutical Classes | Vitamin D [Chemical/Ingredient],Vitamin D Analog [EPC] |