Package 30698-631-05

{"route": ["ORAL"], "spl_id": "3e4799b2-7621-c0b4-e063-6394a90a47b7", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["0Y2S3XUQ5H"], "rxcui": ["197417", "197418", "197419", "205488", "205489", "205490"], "spl_set_id": ["32dfbea3-eb2b-4070-8605-57ce3e6d5a2f"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Validus Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (30698-631-01)", "package_ndc": "30698-631-01", "marketing_start_date": "19830228"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (30698-631-05)", "package_ndc": "30698-631-05", "marketing_start_date": "20240117"}], "brand_name": "Bumex", "product_id": "30698-631_3e4799b2-7621-c0b4-e063-6394a90a47b7", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "30698-631", "generic_name": "Bumetanide", "labeler_name": "Validus Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bumex", "active_ingredients": [{"name": "BUMETANIDE", "strength": "1 mg/1"}], "application_number": "NDA018225", "marketing_category": "NDA", "marketing_start_date": "19830228", "listing_expiration_date": "20261231"}