Package 17224-178-21

{"route": ["ORAL"], "spl_id": "f790f48e-79bb-4d43-e053-6294a90a2b29", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["7LXU5N7ZO5"], "rxcui": ["310429"], "spl_set_id": ["43be0231-0d88-4a21-b2ab-793155cbddb2"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Calvin Scott & Co., Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "21 TABLET in 1 BOTTLE (17224-178-21)", "package_ndc": "17224-178-21", "marketing_start_date": "20160515"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (17224-178-30)", "package_ndc": "17224-178-30", "marketing_start_date": "20160515"}], "brand_name": "Furosemide", "product_id": "17224-178_f790f48e-79bb-4d43-e053-6294a90a2b29", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "17224-178", "generic_name": "FUROSEMIDE", "labeler_name": "Calvin Scott & Co., Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Furosemide", "active_ingredients": [{"name": "FUROSEMIDE", "strength": "20 mg/1"}], "application_number": "ANDA077293", "marketing_category": "ANDA", "marketing_start_date": "20060201", "listing_expiration_date": "20261231"}