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United States · US · US:55513-283_79ccf986-8ff8-4318-9a40-4c5d9f3ae9fd
EPOGEN
UNIISPL
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerAmgen, Inc
CountryUS (United States)
ATC code—
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc11555132831010 VIAL in 1 PACKAGE (55513-283-10) / 2 mL in 1 VIAL (55513-283-01)
- ndc11555132832010 VIAL in 1 PACKAGE (55513-283-20) / 2 mL in 1 VIAL (55513-283-01)
Annotations
UNII (FDA Substance ID)
64FS3BFH5W
EPOETIN
RxCUI 2047589
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "64FS3BFH5W",
"rxcui": "2047589",
"inchikey": null,
"display_name": "EPOETIN",
"substance_type": "protein",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "INTRAVENOUS; SUBCUTANEOUS",
"spl_meta": {
"1f2d0b28-9cc5-4523-80b8-637fdaf3f7a5": {
"match": "brand_token",
"title": "EPOGEN (EPOETIN ALFA) SOLUTION [AMGEN, INC]",
"spl_version": "136",
"published_date": "2025-11-17"
}
},
"productid": "55513-283_79ccf986-8ff8-4318-9a40-4c5d9f3ae9fd",
"productndc": "55513-283",
"dosage_form": "SOLUTION",
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "EPOETIN",
"proprietary_name": "EPOGEN",
"active_ingred_unit": "[iU]/mL",
"application_number": "BLA103234",
"marketing_category": "BLA",
"nonproprietary_name": "epoetin alfa",
"start_marketing_date": "19941205",
"active_numerator_strength": "10000"
}Access this data programmatically
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