U.S. flag

An official website of the United States government

Purple Book
Database of Licensed Biological Products

Product Details for: Epogen/Procrit, Procrit
Product Label Grayed out Product Label links indicate that there is no product label available for the product.

Product NumberDosage FormRoute of AdministrationStrengthProduct PresentationLicense TypeProprietary NameMarketing Status
001Injection Intravenous, Subcutaneous 10,000UNITS/MLSingle-Dose Vial351(a)Epogen/ProcritRx
002Injection Intravenous, Subcutaneous 20,000UNITS/2ML (10,000UNITS/ML)Multi-Dose Vial351(a)Epogen/ProcritRx
003Injection Intravenous, Subcutaneous 20,000UNITS/MLMulti-Dose Vial351(a)Epogen/ProcritRx
004Injection Intravenous, Subcutaneous 2,000UNITS/MLSingle-Dose Vial351(a)Epogen/ProcritRx
005Injection Intravenous, Subcutaneous 3,000UNITS/MLSingle-Dose Vial351(a)Epogen/ProcritRx
006Injection Intravenous, Subcutaneous 40,000UNITS/MLSingle-Dose Vial351(a)ProcritRx
007Injection Intravenous, Subcutaneous 4,000UNITS/MLSingle-Dose Vial351(a)Epogen/ProcritRx

Proper Name
epoetin alfa

BLA Number
103234

Applicant
Amgen Inc.

Original Approval Date
June 1, 1989

Date of First Licensure