Package 50242-087-01

Brand: kadcyla

Generic: ado-trastuzumab emtansine
NDC Package

Package Facts

Identity

Package NDC 50242-087-01
Digits Only 5024208701
Product NDC 50242-087
Description

1 VIAL, SINGLE-USE in 1 CARTON (50242-087-01) / 8 mL in 1 VIAL, SINGLE-USE

Marketing

Marketing Status
Marketed Since 2013-02-22
Brand kadcyla
Generic ado-trastuzumab emtansine
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "b5871dd4-8ade-461c-a4f2-7c71c2fc8393", "openfda": {"unii": ["SE2KH7T06F"], "rxcui": ["1658084", "1658087", "1658089", "1658091"], "spl_set_id": ["23f3c1f4-0fc8-4804-a9e3-04cf25dd302e"], "manufacturer_name": ["Genentech, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-USE in 1 CARTON (50242-087-01)  / 8 mL in 1 VIAL, SINGLE-USE", "package_ndc": "50242-087-01", "marketing_start_date": "20130222"}], "brand_name": "KADCYLA", "product_id": "50242-087_b5871dd4-8ade-461c-a4f2-7c71c2fc8393", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "product_ndc": "50242-087", "generic_name": "ADO-TRASTUZUMAB EMTANSINE", "labeler_name": "Genentech, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "KADCYLA", "active_ingredients": [{"name": "TRASTUZUMAB EMTANSINE", "strength": "20 mg/mL"}], "application_number": "BLA125427", "marketing_category": "BLA", "marketing_start_date": "20130222", "listing_expiration_date": "20261231"}