Package 50242-088-01
Brand: kadcyla
Generic: ado-trastuzumab emtansinePackage Facts
Identity
Package NDC
50242-088-01
Digits Only
5024208801
Product NDC
50242-088
Description
1 VIAL, SINGLE-USE in 1 CARTON (50242-088-01) / 5 mL in 1 VIAL, SINGLE-USE
Marketing
Marketing Status
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 (50242-088-01) / 5 mL in 1 VIAL, SINGLE-USE", "package_ndc": "50242-088-01", "marketing_start_date": "20130222"}], "brand_name": "KADCYLA", "product_id": "50242-088_b5871dd4-8ade-461c-a4f2-7c71c2fc8393", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "product_ndc": "50242-088", "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"}