Product NDC: | 58468-0123 |
Proprietary Name: | Hectorol |
Non Proprietary Name: | DOXERCALCIFEROL |
Active Ingredient(s): | 4 ug/2mL & nbsp; DOXERCALCIFEROL |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 58468-0123 |
Labeler Name: | Genzyme Corporation |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA021027 |
Marketing Category: | NDA |
Start Marketing Date: | 20081208 |
Package NDC: | 58468-0123-1 |
Package Description: | 50 VIAL in 1 BOX (58468-0123-1) > 2 mL in 1 VIAL |
NDC Code | 58468-0123-1 |
Proprietary Name | Hectorol |
Package Description | 50 VIAL in 1 BOX (58468-0123-1) > 2 mL in 1 VIAL |
Product NDC | 58468-0123 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | DOXERCALCIFEROL |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 20081208 |
Marketing Category Name | NDA |
Labeler Name | Genzyme Corporation |
Substance Name | DOXERCALCIFEROL |
Strength Number | 4 |
Strength Unit | ug/2mL |
Pharmaceutical Classes | Ergocalciferols [Chemical/Ingredient],Vitamin D2 Analog [EPC] |