Visitor Monitoring Drug Details: EPOGEN/PROCRIT
 
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Drug Details

Drug Name: EPOGEN/PROCRIT
FDA Application No: (BLA) 103234
Active Ingredient(s): EPOETIN ALFA
Company: AMGEN
Original Approval or Tentative Approval Date: June 1, 1989
 
There are no Therapeutic Equivalents Label Information
Approval History, Letters, Reviews and Related Documents
 
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Drug NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
EPOGEN/PROCRIT EPOETIN ALFA10,000U/MLVIAL; SINGLE-USE Prescription No None
EPOGEN/PROCRIT EPOETIN ALFA20,000U/2MLVIAL; MULTIDOSE Prescription No None
EPOGEN/PROCRIT EPOETIN ALFA20,000/MLVIAL; MULTIDOSE Prescription No None
EPOGEN/PROCRIT EPOETIN ALFA2,000U/MLVIAL; SINGLE-USE Prescription No None
EPOGEN/PROCRIT EPOETIN ALFA3,000U/MLVIAL; SINGLE-USE Prescription No None
EPOGEN/PROCRIT EPOETIN ALFA40,000U/MLVIAL; SINGLE-USE Prescription No None
EPOGEN/PROCRIT EPOETIN ALFA4,000U/MLVIAL; SINGLE-USE Prescription No None


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