Package 43547-423-09

{"route": ["ORAL"], "spl_id": "0be72eb2-c56a-4721-8cb5-d9b778c3e179", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0343547424091", "0343547425098", "0343547423094"], "unii": ["0J48LPH2TH", "3ST302B24A"], "rxcui": ["979464", "979468", "979471"], "spl_set_id": ["6d677f9e-c0e4-4d6e-bea2-a58e986e4635"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Solco Healthcare US, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (43547-423-03)", "package_ndc": "43547-423-03", "marketing_start_date": "20180215"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (43547-423-09)", "package_ndc": "43547-423-09", "marketing_start_date": "20180215"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (43547-423-11)", "package_ndc": "43547-423-11", "marketing_start_date": "20180215"}], "brand_name": "Losartan Potassium and Hydrochlorothiazide", "product_id": "43547-423_0be72eb2-c56a-4721-8cb5-d9b778c3e179", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]", "Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "43547-423", "generic_name": "losartan potassium and hydrochlorothiazide", "labeler_name": "Solco Healthcare US, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Losartan Potassium and Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "12.5 mg/1"}, {"name": "LOSARTAN POTASSIUM", "strength": "50 mg/1"}], "application_number": "ANDA204901", "marketing_category": "ANDA", "marketing_start_date": "20180215", "listing_expiration_date": "20271231"}