Package 50742-366-30

Brand: gefitinib

Generic: gefitinib
NDC Package

Package Facts

Identity

Package NDC 50742-366-30
Digits Only 5074236630
Product NDC 50742-366
Description

30 TABLET, COATED in 1 BOTTLE (50742-366-30)

Marketing

Marketing Status
Marketed Since 2023-04-27
Brand gefitinib
Generic gefitinib
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "932e3701-75ae-438f-bb6a-2c2662c73ee5", "openfda": {"nui": ["N0000175605", "N0000175076"], "unii": ["S65743JHBS"], "rxcui": ["349472"], "spl_set_id": ["6402435f-9f6a-4f02-91a2-6267d783fa78"], "pharm_class_epc": ["Kinase Inhibitor [EPC]"], "pharm_class_moa": ["Protein Kinase Inhibitors [MoA]"], "manufacturer_name": ["Ingenus Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE (50742-366-30)", "package_ndc": "50742-366-30", "marketing_start_date": "20230427"}], "brand_name": "Gefitinib", "product_id": "50742-366_932e3701-75ae-438f-bb6a-2c2662c73ee5", "dosage_form": "TABLET, COATED", "pharm_class": ["Kinase Inhibitor [EPC]", "Protein Kinase Inhibitors [MoA]"], "product_ndc": "50742-366", "generic_name": "Gefitinib", "labeler_name": "Ingenus Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gefitinib", "active_ingredients": [{"name": "GEFITINIB", "strength": "250 mg/1"}], "application_number": "ANDA211591", "marketing_category": "ANDA", "marketing_start_date": "20230427", "listing_expiration_date": "20261231"}