actemra

Generic: tocilizumab

Labeler: genentech, inc.
NDC Directory HUMAN PRESCRIPTION DRUG BLA Inactive Finished

Drug Facts

Product Profile

Brand Name actemra
Generic Name tocilizumab
Labeler genentech, inc.
Dosage Form INJECTION, SOLUTION, CONCENTRATE
Routes
INTRAVENOUS
Active Ingredients

tocilizumab 200 mg/10mL

Manufacturer
Genentech, Inc.

Identifiers & Regulatory

Product NDC 50242-136
Product ID 50242-136_7f1b03d3-e0e1-4d90-b588-bb8d3ecb154a
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category BLA
Application Number BLA125276
Listing Expiration 2026-12-31
Marketing Start 2010-01-08

Pharmacologic Class

Established (EPC)
interleukin-6 receptor antagonist [epc]
Mechanism of Action
interleukin 6 receptor antagonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 50242136
Hyphenated Format 50242-136

Supplemental Identifiers

RxCUI
1441527 1441530 1657974 1657976 1657979 1657980 1657981 1657982 2106073 2106075
UNII
I031V2H011
NUI
N0000190478 N0000190480

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name actemra (source: ndc)
Generic Name tocilizumab (source: ndc)
Application Number BLA125276 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 200 mg/10mL
source: ndc
Packaging
  • 1 VIAL, SINGLE-USE in 1 BOX (50242-136-01) / 10 mL in 1 VIAL, SINGLE-USE
source: ndc

Packages (1)

50242-136-01 1 VIAL, SINGLE-USE in 1 BOX (50242-136-01) / 10 mL in 1 VIAL, SINGLE-USE

Ingredients (1)

tocilizumab (200 mg/10mL)

Linked Drug Pages (1)

ACTEMRA, Actemra, Actemra ACTPen ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "7f1b03d3-e0e1-4d90-b588-bb8d3ecb154a", "openfda": {"nui": ["N0000190478", "N0000190480"], "unii": ["I031V2H011"], "rxcui": ["1441527", "1441530", "1657974", "1657976", "1657979", "1657980", "1657981", "1657982", "2106073", "2106075"], "spl_set_id": ["2e5365ff-cb2a-4b16-b2c7-e35c6bf2de13"], "pharm_class_epc": ["Interleukin-6 Receptor Antagonist [EPC]"], "pharm_class_moa": ["Interleukin 6 Receptor Antagonists [MoA]"], "manufacturer_name": ["Genentech, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-USE in 1 BOX (50242-136-01)  / 10 mL in 1 VIAL, SINGLE-USE", "package_ndc": "50242-136-01", "marketing_start_date": "20100108"}], "brand_name": "ACTEMRA", "product_id": "50242-136_7f1b03d3-e0e1-4d90-b588-bb8d3ecb154a", "dosage_form": "INJECTION, SOLUTION, CONCENTRATE", "pharm_class": ["Interleukin 6 Receptor Antagonists [MoA]", "Interleukin-6 Receptor Antagonist [EPC]"], "product_ndc": "50242-136", "generic_name": "tocilizumab", "labeler_name": "Genentech, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ACTEMRA", "active_ingredients": [{"name": "TOCILIZUMAB", "strength": "200 mg/10mL"}], "application_number": "BLA125276", "marketing_category": "BLA", "marketing_start_date": "20100108", "listing_expiration_date": "20261231"}