Product NDC: | 55513-006 |
Proprietary Name: | ARANESP |
Non Proprietary Name: | darbepoetin alfa |
Active Ingredient(s): | 200 ug/mL & nbsp; darbepoetin alfa |
Administration Route(s): | INTRAVENOUS; SUBCUTANEOUS |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 55513-006 |
Labeler Name: | Amgen Inc |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | BLA103951 |
Marketing Category: | BLA |
Start Marketing Date: | 20060911 |
Package NDC: | 55513-006-01 |
Package Description: | 1 VIAL, SINGLE-DOSE in 1 PACKAGE (55513-006-01) > 1 mL in 1 VIAL, SINGLE-DOSE |
NDC Code | 55513-006-01 |
Proprietary Name | ARANESP |
Package Description | 1 VIAL, SINGLE-DOSE in 1 PACKAGE (55513-006-01) > 1 mL in 1 VIAL, SINGLE-DOSE |
Product NDC | 55513-006 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | darbepoetin alfa |
Dosage Form Name | SOLUTION |
Route Name | INTRAVENOUS; SUBCUTANEOUS |
Start Marketing Date | 20060911 |
Marketing Category Name | BLA |
Labeler Name | Amgen Inc |
Substance Name | DARBEPOETIN ALFA |
Strength Number | 200 |
Strength Unit | ug/mL |
Pharmaceutical Classes | Erythropoiesis-stimulating Agent [EPC],Erythropoietin [Chemical/Ingredient],Increased Erythroid Cell Production [PE] |