Package 42291-035-15

Brand: lapatinib

Generic: lapatinib
NDC Package

Package Facts

Identity

Package NDC 42291-035-15
Digits Only 4229103515
Product NDC 42291-035
Product ID 42291-035_302a4314-e1d6-3ce6-e063-6394a90a75a1
Description

150 TABLET, FILM COATED in 1 BOTTLE (42291-035-15)

Marketing

Marketing Status
Marketed Since 2025-03-12
Brand lapatinib
Generic lapatinib
Sample Package No

Linked Drug Pages (1)

Lapatinib ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "302a4314-e1d6-3ce6-e063-6394a90a75a1", "openfda": {"upc": ["0342291035157"], "unii": ["G873GX646R"], "rxcui": ["672149"], "spl_set_id": ["302a4346-a68d-af3e-e063-6294a90a4a6f"], "manufacturer_name": ["AvKARE"]}, "finished": true, "packaging": [{"sample": false, "description": "150 TABLET, FILM COATED in 1 BOTTLE (42291-035-15)", "package_ndc": "42291-035-15", "marketing_start_date": "20250312"}], "brand_name": "Lapatinib", "product_id": "42291-035_302a4314-e1d6-3ce6-e063-6394a90a75a1", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Kinase Inhibitor [EPC]", "Protein Kinase Inhibitors [MoA]"], "product_ndc": "42291-035", "generic_name": "Lapatinib", "labeler_name": "AvKARE", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lapatinib", "active_ingredients": [{"name": "LAPATINIB DITOSYLATE", "strength": "250 mg/1"}], "application_number": "ANDA217968", "marketing_category": "ANDA", "marketing_start_date": "20250312", "listing_expiration_date": "20261231"}