🇺🇸
United States · US · US:50242-138_7f1b03d3-e0e1-4d90-b588-bb8d3ecb154a
Actemra
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
- ndc1150242138011 SYRINGE, GLASS in 1 BOX (50242-138-01) / .9 mL in 1 SYRINGE, GLASS
- ndc1150242138861 SYRINGE, GLASS in 1 BOX (50242-138-86) / .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": "50242-138_7f1b03d3-e0e1-4d90-b588-bb8d3ecb154a",
"productndc": "50242-138",
"dosage_form": "INJECTION, SOLUTION",
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "TOCILIZUMAB",
"proprietary_name": "Actemra",
"active_ingred_unit": "mg/.9mL",
"application_number": "BLA125472",
"marketing_category": "BLA",
"nonproprietary_name": "tocilizumab",
"start_marketing_date": "20131021",
"active_numerator_strength": "162"
}Related drugs
Other records sharing ATC code L04AC07.
Access this data programmatically
Query Actemra and 610,000+ other drug records through a single REST API — with a last_synced_at provenance stamp on every response. Free tier includes 100 requests/day.