Product NDC: | 0074-1658 |
Proprietary Name: | Zemplar |
Non Proprietary Name: | Paricalcitol |
Active Ingredient(s): | 5 ug/mL & nbsp; Paricalcitol |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0074-1658 |
Labeler Name: | Abbott Laboratories |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA020819 |
Marketing Category: | NDA |
Start Marketing Date: | 19980417 |
Package NDC: | 0074-1658-01 |
Package Description: | 25 VIAL, SINGLE-DOSE in 1 TRAY (0074-1658-01) > 1 mL in 1 VIAL, SINGLE-DOSE |
NDC Code | 0074-1658-01 |
Proprietary Name | Zemplar |
Package Description | 25 VIAL, SINGLE-DOSE in 1 TRAY (0074-1658-01) > 1 mL in 1 VIAL, SINGLE-DOSE |
Product NDC | 0074-1658 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Paricalcitol |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 19980417 |
Marketing Category Name | NDA |
Labeler Name | Abbott Laboratories |
Substance Name | PARICALCITOL |
Strength Number | 5 |
Strength Unit | ug/mL |
Pharmaceutical Classes | Cholecalciferol [Chemical/Ingredient],Vitamin D3 Analog [EPC] |