Package 0078-0671-19

Brand: tykerb

Generic: lapatinib
NDC Package

Package Facts

Identity

Package NDC 0078-0671-19
Digits Only 0078067119
Product NDC 0078-0671
Product ID 0078-0671_940eccaf-92b4-4562-8579-24a53c1bc48d
Description

150 TABLET in 1 BOTTLE (0078-0671-19)

Marketing

Marketing Status
Marketed Since 2016-08-03
Brand tykerb
Generic lapatinib
Sample Package No

Linked Drug Pages (1)

TYKERB ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "940eccaf-92b4-4562-8579-24a53c1bc48d", "openfda": {"unii": ["G873GX646R"], "rxcui": ["672149", "672152"], "spl_set_id": ["eee37f88-ec6a-4c30-b8aa-e2c71f93088c"], "manufacturer_name": ["Novartis Pharmaceuticals Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "150 TABLET in 1 BOTTLE (0078-0671-19)", "package_ndc": "0078-0671-19", "marketing_start_date": "20160803"}], "brand_name": "TYKERB", "product_id": "0078-0671_940eccaf-92b4-4562-8579-24a53c1bc48d", "dosage_form": "TABLET", "pharm_class": ["Kinase Inhibitor [EPC]", "Protein Kinase Inhibitors [MoA]"], "product_ndc": "0078-0671", "generic_name": "lapatinib", "labeler_name": "Novartis Pharmaceuticals Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "TYKERB", "active_ingredients": [{"name": "LAPATINIB DITOSYLATE", "strength": "250 mg/1"}], "application_number": "NDA022059", "marketing_category": "NDA", "marketing_start_date": "20160803", "listing_expiration_date": "20271231"}