Package 72162-1362-1

{"route": ["ORAL"], "spl_id": "babd8961-f2c4-4be1-ae01-8d73fc6a0a3d", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["7LXU5N7ZO5"], "rxcui": ["197732"], "spl_set_id": ["a5e94bf3-bb18-4c81-98af-8c1cb7e00496"], "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": "100 TABLET in 1 BOTTLE, PLASTIC (72162-1362-1)", "package_ndc": "72162-1362-1", "marketing_start_date": "20240202"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE, PLASTIC (72162-1362-5)", "package_ndc": "72162-1362-5", "marketing_start_date": "20240202"}], "brand_name": "Furosemide", "product_id": "72162-1362_babd8961-f2c4-4be1-ae01-8d73fc6a0a3d", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "72162-1362", "generic_name": "furosemide", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Furosemide", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "80 mg/1"}], "application_number": "ANDA076796", "marketing_category": "ANDA", "marketing_start_date": "20040326", "listing_expiration_date": "20261231"}