| Product NDC: | 17478-931 |
| Proprietary Name: | Calcitriol |
| Non Proprietary Name: | Calcitriol |
| Active Ingredient(s): | 1 ug/mL & nbsp; Calcitriol |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 17478-931 |
| Labeler Name: | Akorn, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA078066 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20111014 |
| Package NDC: | 17478-931-01 |
| Package Description: | 10 AMPULE in 1 CARTON (17478-931-01) > 1 mL in 1 AMPULE |
| NDC Code | 17478-931-01 |
| Proprietary Name | Calcitriol |
| Package Description | 10 AMPULE in 1 CARTON (17478-931-01) > 1 mL in 1 AMPULE |
| Product NDC | 17478-931 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Calcitriol |
| Dosage Form Name | INJECTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20111014 |
| Marketing Category Name | ANDA |
| Labeler Name | Akorn, Inc. |
| Substance Name | CALCITRIOL |
| Strength Number | 1 |
| Strength Unit | ug/mL |
| Pharmaceutical Classes | Cholecalciferol [Chemical/Ingredient],Vitamin D3 Analog [EPC] |