Package 50090-3561-0

{"route": ["ORAL"], "spl_id": "14f2f5f6-c610-4338-98bf-7f3f87f4452f", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH", "6M97XTV3HD"], "rxcui": ["403854"], "spl_set_id": ["fe49d96e-5874-4b11-9323-b4a92e9c25dc"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-3561-0)", "package_ndc": "50090-3561-0", "marketing_start_date": "20180830"}], "brand_name": "Olmesartan Medoxomil and Hydrochlorothiazide", "product_id": "50090-3561_14f2f5f6-c610-4338-98bf-7f3f87f4452f", "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": "50090-3561", "generic_name": "Olmesartan Medoxomil and Hydrochlorothiazide", "labeler_name": "A-S Medication Solutions", "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": "40 mg/1"}], "application_number": "ANDA205391", "marketing_category": "ANDA", "marketing_start_date": "20170424", "listing_expiration_date": "20261231"}