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] |