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United States · US · US:55513-023_7023e5d7-0f00-4fa4-8223-fa77bee46feb
ARANESP
UNIISPLATC B03XA02
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerAmgen, Inc
CountryUS (United States)
ATC codeB03XA02
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1155513023041 BLISTER PACK in 1 PACKAGE (55513-023-04) / 4 SYRINGE in 1 BLISTER PACK / .3 mL in 1 SYRINGE (55513-023-01)
Annotations
UNII (FDA Substance ID)
15UQ94PT4P
DARBEPOETIN ALFA
RxCUI 283838
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "15UQ94PT4P",
"rxcui": "283838",
"inchikey": null,
"display_name": "DARBEPOETIN ALFA",
"substance_type": "protein",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "INTRAVENOUS; SUBCUTANEOUS",
"spl_meta": {
"0fd36cb9-c4f6-4167-93c9-8530865db3f9": {
"match": "brand_token",
"title": "ARANESP (DARBEPOETIN ALFA) INJECTION, SOLUTION ARANESP (DARBEPOETIN ALFA) SOLUTION [AMGEN, INC]",
"spl_version": "159",
"published_date": "2026-03-12"
}
},
"productid": "55513-023_7023e5d7-0f00-4fa4-8223-fa77bee46feb",
"productndc": "55513-023",
"dosage_form": "INJECTION, SOLUTION",
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "DARBEPOETIN ALFA",
"proprietary_name": "ARANESP",
"active_ingred_unit": "ug/.3mL",
"application_number": "BLA103951",
"marketing_category": "BLA",
"nonproprietary_name": "darbepoetin alfa",
"start_marketing_date": "20060814",
"active_numerator_strength": "60"
}Related drugs
Other records sharing ATC code B03XA02.
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