Package 72162-1360-0

{"route": ["ORAL"], "spl_id": "22202f87-ad58-420f-a081-22d646c8e7a8", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["7LXU5N7ZO5"], "rxcui": ["310429"], "spl_set_id": ["d07ff11c-c1ab-41e6-a455-f2b89340106e"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE, PLASTIC (72162-1360-0)", "package_ndc": "72162-1360-0", "marketing_start_date": "20240202"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (72162-1360-1)", "package_ndc": "72162-1360-1", "marketing_start_date": "20240202"}], "brand_name": "Furosemide", "product_id": "72162-1360_22202f87-ad58-420f-a081-22d646c8e7a8", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "72162-1360", "generic_name": "furosemide", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Furosemide", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "20 mg/1"}], "application_number": "ANDA076796", "marketing_category": "ANDA", "marketing_start_date": "20040326", "listing_expiration_date": "20261231"}