Package 43353-288-09

{"route": ["ORAL"], "spl_id": "b1b7dc90-3e5c-48cf-8a65-446c52e79d53", "openfda": {"nui": ["N0000175366", "N0000175590"], "unii": ["0Y2S3XUQ5H"], "rxcui": ["197418"], "spl_set_id": ["7e47e7b1-d28a-4e12-882f-cf193b7f2697"], "pharm_class_pe": ["Increased Diuresis at Loop of Henle [PE]"], "pharm_class_epc": ["Loop Diuretic [EPC]"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "9000 TABLET in 1 BOTTLE (43353-288-09)", "package_ndc": "43353-288-09", "marketing_start_date": "20170310"}], "brand_name": "Bumetanide", "product_id": "43353-288_b1b7dc90-3e5c-48cf-8a65-446c52e79d53", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis at Loop of Henle [PE]", "Loop Diuretic [EPC]"], "product_ndc": "43353-288", "generic_name": "Bumetanide", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bumetanide", "active_ingredients": [{"name": "BUMETANIDE", "strength": "1 mg/1"}], "application_number": "ANDA074700", "marketing_category": "ANDA", "marketing_start_date": "19961121", "listing_expiration_date": "20261231"}