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United States · US · US:50242-143_7f1b03d3-e0e1-4d90-b588-bb8d3ecb154a
Actemra ACTPen
UNIISPLATC L04AC07
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerGenentech, Inc.
CountryUS (United States)
ATC codeL04AC07
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 2
- ndc1150242143011 SYRINGE, GLASS in 1 BOX (50242-143-01) / .9 mL in 1 SYRINGE, GLASS
- ndc1150242143861 SYRINGE, GLASS in 1 BOX (50242-143-86) / .9 mL in 1 SYRINGE, GLASS
Annotations
UNII (FDA Substance ID)
I031V2H011
TOCILIZUMAB
RxCUI 612865
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "I031V2H011",
"rxcui": "612865",
"inchikey": null,
"display_name": "TOCILIZUMAB",
"substance_type": "protein",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "SUBCUTANEOUS",
"spl_meta": {
"2e5365ff-cb2a-4b16-b2c7-e35c6bf2de13": {
"match": "brand_token",
"title": "ACTEMRA (TOCILIZUMAB) INJECTION, SOLUTION, CONCENTRATE ACTEMRA (TOCILIZUMAB) INJECTION, SOLUTION ACTEMRA ACTPEN (TOCILIZUMAB) INJECTION, SOLUTION [GENENTECH, INC.]",
"spl_version": "53",
"published_date": "2025-12-19"
}
},
"productid": "50242-143_7f1b03d3-e0e1-4d90-b588-bb8d3ecb154a",
"productndc": "50242-143",
"dosage_form": "INJECTION, SOLUTION",
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "TOCILIZUMAB",
"proprietary_name": "Actemra ACTPen",
"active_ingred_unit": "mg/.9mL",
"application_number": "BLA125472",
"marketing_category": "BLA",
"nonproprietary_name": "tocilizumab",
"start_marketing_date": "20181119",
"active_numerator_strength": "162"
}Related drugs
Other records sharing ATC code L04AC07.
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