| Product NDC: | 45802-608 |
| Proprietary Name: | calcitriol |
| Non Proprietary Name: | calcitriol |
| Active Ingredient(s): | 3 ug/g & nbsp; calcitriol |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | OINTMENT |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 45802-608 |
| Labeler Name: | Perrigo New York Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA022087 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20120308 |
| Package NDC: | 45802-608-01 |
| Package Description: | 1 TUBE in 1 CARTON (45802-608-01) > 100 g in 1 TUBE |
| NDC Code | 45802-608-01 |
| Proprietary Name | calcitriol |
| Package Description | 1 TUBE in 1 CARTON (45802-608-01) > 100 g in 1 TUBE |
| Product NDC | 45802-608 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | calcitriol |
| Dosage Form Name | OINTMENT |
| Route Name | TOPICAL |
| Start Marketing Date | 20120308 |
| Marketing Category Name | NDA |
| Labeler Name | Perrigo New York Inc |
| Substance Name | CALCITRIOL |
| Strength Number | 3 |
| Strength Unit | ug/g |
| Pharmaceutical Classes | Cholecalciferol [Chemical/Ingredient],Vitamin D3 Analog [EPC] |