Package 63539-193-30

Brand: bosulif

Generic: bosutinib
NDC Package

Package Facts

Identity

Package NDC 63539-193-30
Digits Only 6353919330
Product NDC 63539-193
Product ID 63539-193_936ca777-7c42-4d88-a084-002df2b95f1c
Description

30 TABLET, FILM COATED in 1 BOTTLE (63539-193-30)

Marketing

Marketing Status
Marketed Since 2018-02-21
Brand bosulif
Generic bosutinib
Sample Package No

Linked Drug Pages (1)

BOSULIF ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "936ca777-7c42-4d88-a084-002df2b95f1c", "openfda": {"unii": ["844ZJE6I55"], "rxcui": ["1307624", "1307630", "1987732", "1987734"], "spl_set_id": ["d5929f91-6496-4c0e-97e8-0bd524e15763"], "manufacturer_name": ["U.S. Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (63539-193-30)", "package_ndc": "63539-193-30", "marketing_start_date": "20180221"}], "brand_name": "BOSULIF", "product_id": "63539-193_936ca777-7c42-4d88-a084-002df2b95f1c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Bcr-Abl Tyrosine Kinase Inhibitors [MoA]", "Kinase Inhibitor [EPC]"], "product_ndc": "63539-193", "generic_name": "Bosutinib", "labeler_name": "U.S. Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "BOSULIF", "active_ingredients": [{"name": "BOSUTINIB MONOHYDRATE", "strength": "400 mg/1"}], "application_number": "NDA203341", "marketing_category": "NDA", "marketing_start_date": "20120904", "listing_expiration_date": "20261231"}