Package 63539-197-90

Brand: vizimpro

Generic: dacomitinib
NDC Package

Package Facts

Identity

Package NDC 63539-197-90
Digits Only 6353919790
Product NDC 63539-197
Product ID 63539-197_b0b607d1-7a3d-40a2-bf2e-b7eb0f00f762
Description

90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (63539-197-90)

Marketing

Marketing Status
Marketed Since 2019-02-01
Brand vizimpro
Generic dacomitinib
Sample Package No

Linked Drug Pages (1)

Vizimpro ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "b0b607d1-7a3d-40a2-bf2e-b7eb0f00f762", "openfda": {"unii": ["5092U85G58"], "rxcui": ["2058915", "2058922"], "spl_set_id": ["90da33c1-5689-4b4d-a2b5-377e1057a843"], "manufacturer_name": ["U.S. Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (63539-197-90)", "package_ndc": "63539-197-90", "marketing_start_date": "20190201"}], "brand_name": "Vizimpro", "product_id": "63539-197_b0b607d1-7a3d-40a2-bf2e-b7eb0f00f762", "dosage_form": "TABLET, FILM COATED", "product_ndc": "63539-197", "generic_name": "dacomitinib", "labeler_name": "U.S. Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Vizimpro", "active_ingredients": [{"name": "DACOMITINIB", "strength": "15 mg/1"}], "application_number": "NDA211288", "marketing_category": "NDA", "marketing_start_date": "20190201", "listing_expiration_date": "20261231"}