Package 63020-536-30

Brand: iclusig

Generic: ponatinib hydrochloride
NDC Package

Package Facts

Identity

Package NDC 63020-536-30
Digits Only 6302053630
Product NDC 63020-536
Description

30 TABLET, FILM COATED in 1 BOTTLE (63020-536-30)

Marketing

Marketing Status
Marketed Since 2021-01-11
Brand iclusig
Generic ponatinib hydrochloride
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "185604c4-00ec-4764-b6e1-cff93f663fe8", "openfda": {"unii": ["96R6PU3D8J"], "rxcui": ["1364352", "1364358", "1364360", "1364362", "1726637", "1726639", "2473040", "2473042"], "spl_set_id": ["16d804b6-4957-43ee-b18c-3b36ec37c5ac"], "manufacturer_name": ["Takeda Pharmaceuticals America, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (63020-536-30)", "package_ndc": "63020-536-30", "marketing_start_date": "20210111"}], "brand_name": "Iclusig", "product_id": "63020-536_185604c4-00ec-4764-b6e1-cff93f663fe8", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Kinase Inhibitor [EPC]", "Protein Kinase Inhibitors [MoA]"], "product_ndc": "63020-536", "generic_name": "ponatinib hydrochloride", "labeler_name": "Takeda Pharmaceuticals America, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Iclusig", "active_ingredients": [{"name": "PONATINIB HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "NDA203469", "marketing_category": "NDA", "marketing_start_date": "20210111", "listing_expiration_date": "20261231"}