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United States · US · US:51144-050_a695c1a2-3acc-468b-a829-c8761dc041f6
ADCETRIS
UNIISPLATC L01FX05
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerSEAGEN INC.
CountryUS (United States)
ATC codeL01FX05
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1151144050011 VIAL, SINGLE-DOSE in 1 BOX (51144-050-01) / 10.5 mL in 1 VIAL, SINGLE-DOSE
Annotations
UNII (FDA Substance ID)
7XL5ISS668
BRENTUXIMAB VEDOTIN
RxCUI 1147320
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "7XL5ISS668",
"rxcui": "1147320",
"inchikey": null,
"display_name": "BRENTUXIMAB VEDOTIN",
"substance_type": "protein",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "INTRAVENOUS",
"spl_meta": {
"3904f8dd-1aef-3490-e48f-bd55f32ed67f": {
"match": "brand_token",
"title": "ADCETRIS (BRENTUXIMAB VEDOTIN) INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION [SEAGEN INC.]",
"spl_version": "38",
"published_date": "2025-11-17"
}
},
"productid": "51144-050_a695c1a2-3acc-468b-a829-c8761dc041f6",
"productndc": "51144-050",
"dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION",
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "BRENTUXIMAB VEDOTIN",
"proprietary_name": "ADCETRIS",
"active_ingred_unit": "mg/10.5mL",
"application_number": "BLA125388",
"marketing_category": "BLA",
"nonproprietary_name": "brentuximab vedotin",
"start_marketing_date": "20110825",
"active_numerator_strength": "50"
}Related drugs
Other records sharing ATC code L01FX05.
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