Package 0069-0197-30

Brand: vizimpro

Generic: dacomitinib
NDC Package

Package Facts

Identity

Package NDC 0069-0197-30
Digits Only 0069019730
Product NDC 0069-0197
Product ID 0069-0197_cf672c83-c9d9-4107-bcf1-76d4106537cc
Description

30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0069-0197-30)

Marketing

Marketing Status
Marketed Since 2018-10-04
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": "cf672c83-c9d9-4107-bcf1-76d4106537cc", "openfda": {"upc": ["0300691198308", "0300692299301", "0300690197302"], "unii": ["5092U85G58"], "rxcui": ["2058915", "2058922", "2058924", "2058926", "2058930", "2058932"], "spl_set_id": ["4ab27d2f-e385-4e9c-b324-fa69c10b855a"], "manufacturer_name": ["Pfizer Laboratories Div Pfizer Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0069-0197-30)", "package_ndc": "0069-0197-30", "marketing_start_date": "20181004"}], "brand_name": "Vizimpro", "product_id": "0069-0197_cf672c83-c9d9-4107-bcf1-76d4106537cc", "dosage_form": "TABLET, FILM COATED", "product_ndc": "0069-0197", "generic_name": "dacomitinib", "labeler_name": "Pfizer Laboratories Div Pfizer Inc", "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": "20181004", "listing_expiration_date": "20261231"}