EPOGEN - 55513-478-10 - (epoetin alfa)

Alphabetical Index


Drug Information of EPOGEN

Product NDC: 55513-478
Proprietary Name: EPOGEN
Non Proprietary Name: epoetin alfa
Active Ingredient(s): 20000    [iU]/mL & nbsp;   epoetin alfa
Administration Route(s): INTRAVENOUS; SUBCUTANEOUS
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of EPOGEN

Product NDC: 55513-478
Labeler Name: Amgen Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA103234
Marketing Category: BLA
Start Marketing Date: 19970303

Package Information of EPOGEN

Package NDC: 55513-478-10
Package Description: 10 VIAL in 1 PACKAGE (55513-478-10) > 1 mL in 1 VIAL (55513-478-01)

NDC Information of EPOGEN

NDC Code 55513-478-10
Proprietary Name EPOGEN
Package Description 10 VIAL in 1 PACKAGE (55513-478-10) > 1 mL in 1 VIAL (55513-478-01)
Product NDC 55513-478
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name epoetin alfa
Dosage Form Name SOLUTION
Route Name INTRAVENOUS; SUBCUTANEOUS
Start Marketing Date 19970303
Marketing Category Name BLA
Labeler Name Amgen Inc
Substance Name ERYTHROPOIETIN
Strength Number 20000
Strength Unit [iU]/mL
Pharmaceutical Classes Erythropoiesis-stimulating Agent [EPC],Erythropoietin [Chemical/Ingredient],Increased Erythroid Cell Production [PE]

Complete Information of EPOGEN


General Information