Package 70756-812-12

{"route": ["ORAL"], "spl_id": "45806c19-480f-987e-e063-6394a90aa8fa", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0370756814122"], "unii": ["0J48LPH2TH", "6M97XTV3HD"], "rxcui": ["403853", "403854", "403855"], "spl_set_id": ["9771066e-c05d-6a93-e053-2995a90a7e87"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Lifestar Pharma LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (70756-812-12)", "package_ndc": "70756-812-12", "marketing_start_date": "20201001"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (70756-812-30)", "package_ndc": "70756-812-30", "marketing_start_date": "20201001"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (70756-812-51)", "package_ndc": "70756-812-51", "marketing_start_date": "20201001"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (70756-812-90)", "package_ndc": "70756-812-90", "marketing_start_date": "20201001"}], "brand_name": "Olmesartan Medoxomil and Hydrochlorothiazide", "product_id": "70756-812_45806c19-480f-987e-e063-6394a90aa8fa", "dosage_form": "TABLET", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]", "Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "70756-812", "generic_name": "Olmesartan Medoxomil and Hydrochlorothiazide", "labeler_name": "Lifestar Pharma LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Olmesartan Medoxomil and Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "12.5 mg/1"}, {"name": "OLMESARTAN MEDOXOMIL", "strength": "20 mg/1"}], "application_number": "ANDA208847", "marketing_category": "ANDA", "marketing_start_date": "20201001", "listing_expiration_date": "20261231"}