Product Details for: Epogen/Procrit

RETURN TO SEARCH RESULTS
PRODUCT LABEL Grayed out Product Label links indicate that there is no product label available for the product.
Product Number
Dosage Form
Route of Administration
Strength
Product Presentation
License Type
Proprietary Name
Marketing Status
001
Injection
Intravenous, Subcutaneous
10,000UNITS/ML
Single-Dose Vial
351(a)
Epogen/Procrit
Rx
002
Injection
Intravenous, Subcutaneous
20,000UNITS/2ML (10,000UNITS/ML)
Multi-Dose Vial
351(a)
Epogen/Procrit
Rx
003
Injection
Intravenous, Subcutaneous
20,000UNITS/ML
Multi-Dose Vial
351(a)
Epogen/Procrit
Rx
004
Injection
Intravenous, Subcutaneous
2,000UNITS/ML
Single-Dose Vial
351(a)
Epogen/Procrit
Rx
005
Injection
Intravenous, Subcutaneous
3,000UNITS/ML
Single-Dose Vial
351(a)
Epogen/Procrit
Rx
006
Injection
Intravenous, Subcutaneous
40,000UNITS/ML
Single-Dose Vial
351(a)
Procrit
Rx
007
Injection
Intravenous, Subcutaneous
4,000UNITS/ML
Single-Dose Vial
351(a)
Epogen/Procrit
Rx
Proper Name
epoetin alfa
BLA Number
103234
Applicant
Amgen Inc.
Original Approval Date
June 1, 1989
Date of First Licensure
RETURN TO SEARCH RESULTS