| Product NDC: | 0074-8110 |
| Proprietary Name: | Calcijex |
| Non Proprietary Name: | Calcitriol |
| Active Ingredient(s): | 1 ug/mL & nbsp; Calcitriol |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 0074-8110 |
| Labeler Name: | Abbott Laboratories |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA018874 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20100601 |
| Package NDC: | 0074-8110-31 |
| Package Description: | 5 AMPULE in 1 CARTON (0074-8110-31) > 1 mL in 1 AMPULE |
| NDC Code | 0074-8110-31 |
| Proprietary Name | Calcijex |
| Package Description | 5 AMPULE in 1 CARTON (0074-8110-31) > 1 mL in 1 AMPULE |
| Product NDC | 0074-8110 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Calcitriol |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20100601 |
| Marketing Category Name | NDA |
| Labeler Name | Abbott Laboratories |
| Substance Name | CALCITRIOL |
| Strength Number | 1 |
| Strength Unit | ug/mL |
| Pharmaceutical Classes | Cholecalciferol [Chemical/Ingredient],Vitamin D3 Analog [EPC] |