Package 50242-717-01

Brand: cotellic

Generic: cobimetinib
NDC Package

Package Facts

Identity

Package NDC 50242-717-01
Digits Only 5024271701
Product NDC 50242-717
Product ID 50242-717_f3881f36-9b41-4c3c-a964-f7a3ecc932d1
Description

63 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50242-717-01)

Marketing

Marketing Status
Marketed Since 2015-11-10
Brand cotellic
Generic cobimetinib
Sample Package No

Linked Drug Pages (1)

Cotellic ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "f3881f36-9b41-4c3c-a964-f7a3ecc932d1", "openfda": {"unii": ["6EXI96H8SV"], "rxcui": ["1722370", "1722376"], "spl_set_id": ["c387579e-cee0-4334-bd1e-73f93ac1bde6"], "manufacturer_name": ["Genentech, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "63 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50242-717-01)", "package_ndc": "50242-717-01", "marketing_start_date": "20151110"}], "brand_name": "Cotellic", "product_id": "50242-717_f3881f36-9b41-4c3c-a964-f7a3ecc932d1", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Kinase Inhibitor [EPC]", "Kinase Inhibitors [MoA]"], "product_ndc": "50242-717", "generic_name": "COBIMETINIB", "labeler_name": "Genentech, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cotellic", "active_ingredients": [{"name": "COBIMETINIB FUMARATE", "strength": "20 mg/1"}], "application_number": "NDA206192", "marketing_category": "NDA", "marketing_start_date": "20151110", "listing_expiration_date": "20261231"}