Package 65862-468-39

{"route": ["ORAL"], "spl_id": "194eea48-8bc8-476d-a604-4b656222d5be", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH", "3ST302B24A"], "rxcui": ["979464", "979468", "979471"], "spl_set_id": ["dc177d6c-c754-4379-8c2f-1cf6f52f950a"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 CARTON (65862-468-10)  / 10 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "65862-468-10", "marketing_start_date": "20101006"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (65862-468-30)", "package_ndc": "65862-468-30", "marketing_start_date": "20101006"}, {"sample": false, "description": "3000 TABLET, FILM COATED in 1 BOTTLE (65862-468-39)", "package_ndc": "65862-468-39", "marketing_start_date": "20101006"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (65862-468-90)", "package_ndc": "65862-468-90", "marketing_start_date": "20101006"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (65862-468-99)", "package_ndc": "65862-468-99", "marketing_start_date": "20101006"}], "brand_name": "Losartan Potassium and Hydrochlorothiazide", "product_id": "65862-468_194eea48-8bc8-476d-a604-4b656222d5be", "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": "65862-468", "generic_name": "Losartan Potassium and Hydrochlorothiazide", "labeler_name": "Aurobindo Pharma Limited", "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": "ANDA091629", "marketing_category": "ANDA", "marketing_start_date": "20101006", "listing_expiration_date": "20261231"}