Product NDC: | 17478-932 |
Proprietary Name: | Calcitriol |
Non Proprietary Name: | Calcitriol |
Active Ingredient(s): | 2 ug/mL & nbsp; Calcitriol |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 17478-932 |
Labeler Name: | Akorn, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA078066 |
Marketing Category: | ANDA |
Start Marketing Date: | 20111014 |
Package NDC: | 17478-932-01 |
Package Description: | 10 AMPULE in 1 CARTON (17478-932-01) > 1 mL in 1 AMPULE |
NDC Code | 17478-932-01 |
Proprietary Name | Calcitriol |
Package Description | 10 AMPULE in 1 CARTON (17478-932-01) > 1 mL in 1 AMPULE |
Product NDC | 17478-932 |
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 | 2 |
Strength Unit | ug/mL |
Pharmaceutical Classes | Cholecalciferol [Chemical/Ingredient],Vitamin D3 Analog [EPC] |