epogen
Generic: epoetin alfa
Labeler: amgen, incDrug Facts
Product Profile
Brand Name
epogen
Generic Name
epoetin alfa
Labeler
amgen, inc
Dosage Form
SOLUTION
Routes
Active Ingredients
epoetin 3000 [iU]/mL
Manufacturer
Identifiers & Regulatory
Product NDC
55513-267
Product ID
55513-267_79ccf986-8ff8-4318-9a40-4c5d9f3ae9fd
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
BLA
Application Number
BLA103234
Listing Expiration
2026-12-31
Marketing Start
1990-04-30
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
55513267
Hyphenated Format
55513-267
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
epogen (source: ndc)
Generic Name
epoetin alfa (source: ndc)
Application Number
BLA103234 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 3000 [iU]/mL
Packaging
- 10 VIAL in 1 PACKAGE (55513-267-10) / 1 mL in 1 VIAL (55513-267-01)
- 10 VIAL in 1 PACKAGE (55513-267-20) / 1 mL in 1 VIAL (55513-267-01)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "79ccf986-8ff8-4318-9a40-4c5d9f3ae9fd", "openfda": {"unii": ["64FS3BFH5W"], "rxcui": ["205912", "205917", "205921", "205923", "212218", "239998", "239999", "240000", "240377", "241999", "1721684", "1721685"], "spl_set_id": ["1f2d0b28-9cc5-4523-80b8-637fdaf3f7a5"], "manufacturer_name": ["Amgen, Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 PACKAGE (55513-267-10) / 1 mL in 1 VIAL (55513-267-01)", "package_ndc": "55513-267-10", "marketing_start_date": "19900430"}, {"sample": false, "description": "10 VIAL in 1 PACKAGE (55513-267-20) / 1 mL in 1 VIAL (55513-267-01)", "package_ndc": "55513-267-20", "marketing_start_date": "20250414"}], "brand_name": "EPOGEN", "product_id": "55513-267_79ccf986-8ff8-4318-9a40-4c5d9f3ae9fd", "dosage_form": "SOLUTION", "pharm_class": ["Erythropoiesis-stimulating Agent [EPC]", "Erythropoietin [CS]", "Increased Erythroid Cell Production [PE]"], "product_ndc": "55513-267", "generic_name": "epoetin alfa", "labeler_name": "Amgen, Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "EPOGEN", "active_ingredients": [{"name": "EPOETIN", "strength": "3000 [iU]/mL"}], "application_number": "BLA103234", "marketing_category": "BLA", "marketing_start_date": "19900430", "listing_expiration_date": "20261231"}