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ARANESP
ARANESP - 55513-002-04 - (darbepoetin alfa)
Drug Information of ARANESP
| Product NDC: | 55513-002 |
| Proprietary Name: | ARANESP |
| Non Proprietary Name: | darbepoetin alfa |
| Active Ingredient(s): | 25 ug/mL & nbsp; darbepoetin alfa |
| Administration Route(s): | INTRAVENOUS; SUBCUTANEOUS |
| Dosage Form(s): | SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of ARANESP
| Product NDC: | 55513-002 |
| Labeler Name: | Amgen Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | BLA103951 |
| Marketing Category: | BLA |
| Start Marketing Date: | 20060911 |
Package Information of ARANESP
| Package NDC: | 55513-002-04 |
| Package Description: | 4 VIAL, SINGLE-DOSE in 1 PACKAGE (55513-002-04) > 1 mL in 1 VIAL, SINGLE-DOSE (55513-002-01) |
NDC Information of ARANESP
| NDC Code | 55513-002-04 |
| Proprietary Name | ARANESP |
| Package Description | 4 VIAL, SINGLE-DOSE in 1 PACKAGE (55513-002-04) > 1 mL in 1 VIAL, SINGLE-DOSE (55513-002-01) |
| Product NDC | 55513-002 |
| 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 | 25 |
| Strength Unit | ug/mL |
| Pharmaceutical Classes | Erythropoiesis-stimulating Agent [EPC],Erythropoietin [Chemical/Ingredient],Increased Erythroid Cell Production [PE] |
