Package 50090-7571-0

{"route": ["ORAL"], "spl_id": "ea9e8bfd-6d67-41b6-93af-60ef5adc11c0", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH", "6M97XTV3HD"], "rxcui": ["403854"], "spl_set_id": ["f7415f1d-98c7-454f-bb1a-f59e95652c88"], "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 (50090-7571-0)", "package_ndc": "50090-7571-0", "marketing_start_date": "20250605"}], "brand_name": "OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE", "product_id": "50090-7571_ea9e8bfd-6d67-41b6-93af-60ef5adc11c0", "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": "50090-7571", "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": "ANDA204801", "marketing_category": "ANDA", "marketing_start_date": "20230602", "listing_expiration_date": "20261231"}