Aranesp

Active Ingredient(s): Darbepoetin Alfa
FDA Approved: * September 17, 2001
Pharm Company: * AMGEN
Category: Anemia

Darbepoetin alfa (INN) /drbpotn/ is a re-engineered form of erythropoietin containing 5 amino acid changes (N30, T32, V87, N88, T90) resulting in the creation of 2 new sites for N-linked carbohydrate addition. It has a 3-fold longer serum half-life compared to epoetin alpha and epoetin beta. It stimulates erythropoiesis (increases red blood cell levels) by the same mechanism as rHuEpo (binding and activating the Epo receptor) and is used to treat anemia, commonly associated with chronic kidne... [wikipedia]

* May have multiple approval dates, manufacturers, or labelers.
7 Discussions

Dosage List

Aranesp 25 ug/ml Intravenous; Subcutaneous Solution
NDC: 55513-002
Labeler:
Amgen Inc
Aranesp 40 ug/ml Intravenous; Subcutaneous Solution
NDC: 55513-003
Labeler:
Amgen Inc
Aranesp 60 ug/ml Intravenous; Subcutaneous Solution
NDC: 55513-004
Labeler:
Amgen Inc
Aranesp 100 ug/ml Intravenous; Subcutaneous Solution
NDC: 55513-005
Labeler:
Amgen Inc
Aranesp 200 ug/ml Intravenous; Subcutaneous Solution
NDC: 55513-006
Labeler:
Amgen Inc
Aranesp 40 ug/.4ml Intravenous; Subcutaneous Injection, Solution
NDC: 55513-021
Labeler:
Amgen Inc
Aranesp 60 ug/.3ml Intravenous; Subcutaneous Injection, Solution
NDC: 55513-023
Labeler:
Amgen Inc
Aranesp 100 ug/.5ml Intravenous; Subcutaneous Injection, Solution
NDC: 55513-025
Labeler:
Amgen Inc
Aranesp 150 ug/.3ml Intravenous; Subcutaneous Injection, Solution
NDC: 55513-027
Labeler:
Amgen Inc
Aranesp 200 ug/.4ml Intravenous; Subcutaneous Injection, Solution
NDC: 55513-028
Labeler:
Amgen Inc

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