Package 0591-0424-05

{"route": ["ORAL"], "spl_id": "31975473-b876-48d4-81f4-b322137d8900", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776", "N0000008859", "N0000175418"], "upc": ["0305910424015"], "unii": ["0J48LPH2TH", "WS821Z52LQ"], "rxcui": ["310812", "310818"], "spl_set_id": ["abf2fe45-8b69-4d3c-981e-289c0aa3e98b"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]", "Decreased Renal K+ Excretion [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]", "Potassium-sparing Diuretic [EPC]"], "manufacturer_name": ["Actavis Pharma, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (0591-0424-01)", "package_ndc": "0591-0424-01", "marketing_start_date": "19930923"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE, PLASTIC (0591-0424-05)", "package_ndc": "0591-0424-05", "marketing_start_date": "19930923"}], "brand_name": "Triamterene and Hydrochlorothiazide", "product_id": "0591-0424_31975473-b876-48d4-81f4-b322137d8900", "dosage_form": "TABLET", "pharm_class": ["Decreased Renal K+ Excretion [PE]", "Increased Diuresis [PE]", "Increased Diuresis [PE]", "Potassium-sparing Diuretic [EPC]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "0591-0424", "generic_name": "Triamterene and Hydrochlorothiazide", "labeler_name": "Actavis Pharma, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Triamterene and Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "25 mg/1"}, {"name": "TRIAMTERENE", "strength": "37.5 mg/1"}], "application_number": "ANDA073449", "marketing_category": "ANDA", "marketing_start_date": "19930923", "listing_expiration_date": "20261231"}