Package 70771-1485-9

{"route": ["ORAL"], "spl_id": "be4934db-c496-4b06-84c6-587cb656d5fc", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776", "N0000000070", "N0000175561"], "upc": ["0370771148905"], "unii": ["0J48LPH2TH", "80M03YXJ7I"], "rxcui": ["200284", "200285", "349353", "636042", "636045"], "spl_set_id": ["bd199010-1d85-4011-939c-4704ecfaba1f"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]", "Angiotensin 2 Receptor Blocker [EPC]"], "pharm_class_moa": ["Angiotensin 2 Receptor Antagonists [MoA]"], "manufacturer_name": ["Zydus Lifesciences Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (70771-1485-0)", "package_ndc": "70771-1485-0", "marketing_start_date": "20200212"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (70771-1485-4)  / 10 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "70771-1485-4", "marketing_start_date": "20200212"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (70771-1485-9)", "package_ndc": "70771-1485-9", "marketing_start_date": "20200212"}], "brand_name": "valsartan and hydrochlorothiazide", "product_id": "70771-1485_be4934db-c496-4b06-84c6-587cb656d5fc", "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": "70771-1485", "generic_name": "valsartan and hydrochlorothiazide", "labeler_name": "Zydus Lifesciences Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "valsartan and hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "12.5 mg/1"}, {"name": "VALSARTAN", "strength": "80 mg/1"}], "application_number": "ANDA203000", "marketing_category": "ANDA", "marketing_start_date": "20200212", "listing_expiration_date": "20261231"}