Package 72189-497-30

{"route": ["ORAL"], "spl_id": "4c4b0c1a-d843-08bc-e063-6394a90ad546", "openfda": {"nui": ["N0000175557", "N0000011310"], "unii": ["27O7W4T232"], "rxcui": ["313096"], "spl_set_id": ["ffd2f3f5-c7c8-0028-e053-6394a90aaf17"], "pharm_class_epc": ["Aldosterone Antagonist [EPC]"], "pharm_class_moa": ["Aldosterone Antagonists [MoA]"], "manufacturer_name": ["Direct_Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, COATED in 1 BOTTLE (72189-497-30)", "package_ndc": "72189-497-30", "marketing_start_date": "20230706"}, {"sample": false, "description": "90 TABLET, COATED in 1 BOTTLE (72189-497-90)", "package_ndc": "72189-497-90", "marketing_start_date": "20230706"}], "brand_name": "Spironolactone", "product_id": "72189-497_4c4b0c1a-d843-08bc-e063-6394a90ad546", "dosage_form": "TABLET, COATED", "pharm_class": ["Aldosterone Antagonist [EPC]", "Aldosterone Antagonists [MoA]"], "product_ndc": "72189-497", "generic_name": "Spironolactone", "labeler_name": "Direct_Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Spironolactone", "active_ingredients": [{"name": "SPIRONOLACTONE", "strength": "25 mg/1"}], "application_number": "ANDA040750", "marketing_category": "ANDA", "marketing_start_date": "20230706", "listing_expiration_date": "20271231"}