Package 53489-144-10

{"route": ["ORAL"], "spl_id": "b1902b0c-42e6-4e08-bb4a-959280f33579", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776", "N0000175557", "N0000011310"], "unii": ["0J48LPH2TH", "27O7W4T232"], "rxcui": ["198224"], "spl_set_id": ["d7fa3c79-9f26-415b-8039-eb2acabcf66b"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]", "Aldosterone Antagonist [EPC]"], "pharm_class_moa": ["Aldosterone Antagonists [MoA]"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (53489-144-01)", "package_ndc": "53489-144-01", "marketing_start_date": "19870702"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE, PLASTIC (53489-144-05)", "package_ndc": "53489-144-05", "marketing_start_date": "19870702"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE, PLASTIC (53489-144-10)", "package_ndc": "53489-144-10", "marketing_start_date": "19870702"}], "brand_name": "Spironolactone and Hydrochlorothiazide", "product_id": "53489-144_b1902b0c-42e6-4e08-bb4a-959280f33579", "dosage_form": "TABLET", "pharm_class": ["Aldosterone Antagonist [EPC]", "Aldosterone Antagonists [MoA]", "Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "53489-144", "generic_name": "Spironolactone and Hydrochlorothiazide", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Spironolactone and Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "25 mg/1"}, {"name": "SPIRONOLACTONE", "strength": "25 mg/1"}], "application_number": "ANDA089534", "marketing_category": "ANDA", "marketing_start_date": "19870702", "listing_expiration_date": "20261231"}