Package 82009-024-05

{"route": ["ORAL"], "spl_id": "98acb755-ad5c-414a-b9e9-6cd30c10a2e7", "openfda": {"nui": ["N0000008553", "N0000175911"], "upc": ["0382009024059"], "unii": ["EOR26LQQ24"], "rxcui": ["349556"], "spl_set_id": ["68247ce8-e812-42f2-a3ba-0f6e49acca63"], "pharm_class_pe": ["Decreased Cholesterol Absorption [PE]"], "pharm_class_epc": ["Dietary Cholesterol Absorption Inhibitor [EPC]"], "manufacturer_name": ["Quallent Pharmaceuticals Health LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (82009-024-05)", "package_ndc": "82009-024-05", "marketing_start_date": "20220820"}], "brand_name": "ezetimibe", "product_id": "82009-024_98acb755-ad5c-414a-b9e9-6cd30c10a2e7", "dosage_form": "TABLET", "pharm_class": ["Decreased Cholesterol Absorption [PE]", "Dietary Cholesterol Absorption Inhibitor [EPC]"], "product_ndc": "82009-024", "generic_name": "ezetimibe", "labeler_name": "Quallent Pharmaceuticals Health LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ezetimibe", "active_ingredients": [{"name": "EZETIMIBE", "strength": "10 mg/1"}], "application_number": "ANDA204331", "marketing_category": "ANDA", "marketing_start_date": "20220820", "listing_expiration_date": "20261231"}