Package 0093-7367-56

{"route": ["ORAL"], "spl_id": "3fa33b06-383d-42a5-9349-35d3bdf9ab30", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH", "3ST302B24A"], "rxcui": ["979464", "979468", "979471"], "spl_set_id": ["deafd195-7a1b-4ad8-a371-2cd9f433dea5"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (0093-7367-10)", "package_ndc": "0093-7367-10", "marketing_start_date": "20100406"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (0093-7367-56)", "package_ndc": "0093-7367-56", "marketing_start_date": "20100406"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (0093-7367-98)", "package_ndc": "0093-7367-98", "marketing_start_date": "20100406"}], "brand_name": "Losartan Potassium and Hydrochlorothiazide", "product_id": "0093-7367_3fa33b06-383d-42a5-9349-35d3bdf9ab30", "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": "0093-7367", "generic_name": "Losartan Potassium and Hydrochlorothiazide", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "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": "20271231"}