| Product NDC: | 66993-878 |
| Proprietary Name: | calcipotriene |
| Non Proprietary Name: | calcipotriene |
| Active Ingredient(s): | 50 ug/g & nbsp; calcipotriene |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 66993-878 |
| Labeler Name: | Prasco Laboratories |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020273 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20130701 |
| Package NDC: | 66993-878-78 |
| Package Description: | 50 CARTON in 1 CASE (66993-878-78) > 1 TUBE in 1 CARTON > 120 g in 1 TUBE |
| NDC Code | 66993-878-78 |
| Proprietary Name | calcipotriene |
| Package Description | 50 CARTON in 1 CASE (66993-878-78) > 1 TUBE in 1 CARTON > 120 g in 1 TUBE |
| Product NDC | 66993-878 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | calcipotriene |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 20130701 |
| Marketing Category Name | NDA |
| Labeler Name | Prasco Laboratories |
| Substance Name | CALCIPOTRIENE |
| Strength Number | 50 |
| Strength Unit | ug/g |
| Pharmaceutical Classes | Vitamin D [Chemical/Ingredient],Vitamin D Analog [EPC] |