Package 63187-552-90

{"route": ["ORAL"], "spl_id": "fb8e542d-442d-40f6-b9f6-2d616f048b02", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH", "3ST302B24A"], "rxcui": ["979468"], "spl_set_id": ["7897d182-2859-4a40-af4d-aaa9d9720fd9"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (63187-552-30)", "package_ndc": "63187-552-30", "marketing_start_date": "20100406"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (63187-552-60)", "package_ndc": "63187-552-60", "marketing_start_date": "20100406"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (63187-552-90)", "package_ndc": "63187-552-90", "marketing_start_date": "20100406"}], "brand_name": "Losartan Potassium and Hydrochlorothiazide", "product_id": "63187-552_fb8e542d-442d-40f6-b9f6-2d616f048b02", "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": "63187-552", "generic_name": "Losartan Potassium and Hydrochlorothiazide", "labeler_name": "Proficient Rx LP", "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": "ANDA077157", "marketing_category": "ANDA", "marketing_start_date": "20100406", "listing_expiration_date": "20261231"}