Package 67184-0531-3

Brand: gefitinib

Generic: gefitinib
NDC Package

Package Facts

Identity

Package NDC 67184-0531-3
Digits Only 6718405313
Product NDC 67184-0531
Description

3 BLISTER PACK in 1 CARTON (67184-0531-3) / 10 TABLET, COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2023-02-13
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": "8aa73f33-2813-4dfa-939f-e4291081449a", "openfda": {"nui": ["N0000175605", "N0000175076"], "upc": ["0367184053124"], "unii": ["S65743JHBS"], "rxcui": ["349472"], "spl_set_id": ["0afc12dd-12f8-4def-9027-f38412a862b9"], "pharm_class_epc": ["Kinase Inhibitor [EPC]"], "pharm_class_moa": ["Protein Kinase Inhibitors [MoA]"], "manufacturer_name": ["Qilu Pharmaceutical Co., Ltd."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE (67184-0531-1)", "package_ndc": "67184-0531-1", "marketing_start_date": "20230213"}, {"sample": false, "description": "500 TABLET, COATED in 1 BOTTLE (67184-0531-2)", "package_ndc": "67184-0531-2", "marketing_start_date": "20230213"}, {"sample": false, "description": "3 BLISTER PACK in 1 CARTON (67184-0531-3)  / 10 TABLET, COATED in 1 BLISTER PACK", "package_ndc": "67184-0531-3", "marketing_start_date": "20230213"}], "brand_name": "Gefitinib", "product_id": "67184-0531_8aa73f33-2813-4dfa-939f-e4291081449a", "dosage_form": "TABLET, COATED", "pharm_class": ["Kinase Inhibitor [EPC]", "Protein Kinase Inhibitors [MoA]"], "product_ndc": "67184-0531", "generic_name": "Gefitinib", "labeler_name": "Qilu Pharmaceutical Co., Ltd.", "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": "20230213", "listing_expiration_date": "20261231"}