Product NDC: | 0143-9728 |
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: | 0143-9728 |
Labeler Name: | West-ward Pharmaceutical Corp |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA077102 |
Marketing Category: | ANDA |
Start Marketing Date: | 20060208 |
Package NDC: | 0143-9728-05 |
Package Description: | 1 mL in 1 AMPULE (0143-9728-05) |
NDC Code | 0143-9728-05 |
Proprietary Name | Calcitriol |
Package Description | 1 mL in 1 AMPULE (0143-9728-05) |
Product NDC | 0143-9728 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Calcitriol |
Dosage Form Name | INJECTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 20060208 |
Marketing Category Name | ANDA |
Labeler Name | West-ward Pharmaceutical Corp |
Substance Name | CALCITRIOL |
Strength Number | 1 |
Strength Unit | ug/mL |
Pharmaceutical Classes | Cholecalciferol [Chemical/Ingredient],Vitamin D3 Analog [EPC] |