| 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] |