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United States · US · US:55513-670_6b1480b9-1db9-4bbc-91e3-e967574f2055
AVSOLA
UNIISPLATC L04AB02
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerAmgen, Inc
CountryUS (United States)
ATC codeL04AB02
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc1155513670011 VIAL, SINGLE-DOSE in 1 CARTON (55513-670-01) / 10 mL in 1 VIAL, SINGLE-DOSE
- ndc1155513670211 VIAL, SINGLE-DOSE in 1 CARTON (55513-670-21) / 10 mL in 1 VIAL, SINGLE-DOSE
Annotations
UNII (FDA Substance ID)
B72HH48FLU
INFLIXIMAB
RxCUI 191831
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "B72HH48FLU",
"rxcui": "191831",
"inchikey": null,
"display_name": "INFLIXIMAB",
"substance_type": "protein",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "INTRAVENOUS",
"spl_meta": {
"de34bcb7-b524-45c8-9181-61c6f48d540e": {
"match": "brand_token",
"title": "AVSOLA (INFLIXIMAB-AXXQ) INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION [AMGEN, INC]",
"spl_version": "18",
"published_date": "2025-09-15"
}
},
"productid": "55513-670_6b1480b9-1db9-4bbc-91e3-e967574f2055",
"productndc": "55513-670",
"dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION",
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "INFLIXIMAB",
"proprietary_name": "AVSOLA",
"active_ingred_unit": "mg/10mL",
"application_number": "BLA761086",
"marketing_category": "BLA",
"nonproprietary_name": "infliximab-axxq",
"start_marketing_date": "20191212",
"active_numerator_strength": "100"
}Related drugs
Other records sharing ATC code L04AB02.
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