Package 63539-019-01

Brand: sutent

Generic: sunitinib malate
NDC Package Sample

Package Facts

Identity

Package NDC 63539-019-01
Digits Only 6353901901
Product NDC 63539-019
Product ID 63539-019_21cadbc0-3f0e-4789-80ee-bf1e3982d85f
Description

14 CAPSULE in 1 BOTTLE (63539-019-01)

Marketing

Marketing Status
Marketed Since 2017-05-02
Brand sutent
Generic sunitinib malate
Sample Package Yes

Linked Drug Pages (1)

SUTENT ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "21cadbc0-3f0e-4789-80ee-bf1e3982d85f", "openfda": {"unii": ["LVX8N1UT73"], "rxcui": ["616279", "616283", "616289", "616292"], "spl_set_id": ["a5d555f5-d66a-4f94-abcf-96fa6d71a32f"], "manufacturer_name": ["U.S. Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": true, "description": "14 CAPSULE in 1 BOTTLE (63539-019-01)", "package_ndc": "63539-019-01", "marketing_start_date": "20170502"}], "brand_name": "SUTENT", "product_id": "63539-019_21cadbc0-3f0e-4789-80ee-bf1e3982d85f", "dosage_form": "CAPSULE", "pharm_class": ["Kinase Inhibitor [EPC]", "Protein Kinase Inhibitors [MoA]"], "product_ndc": "63539-019", "generic_name": "Sunitinib malate", "labeler_name": "U.S. Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SUTENT", "active_ingredients": [{"name": "SUNITINIB MALATE", "strength": "50 mg/1"}], "application_number": "NDA021938", "marketing_category": "NDA", "marketing_start_date": "20060126", "listing_expiration_date": "20261231"}