Package 42291-925-90

{"route": ["ORAL"], "spl_id": "48bfa982-5678-139d-e063-6294a90adbfa", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0342291925908", "0342291924901"], "unii": ["0J48LPH2TH", "6M97XTV3HD"], "rxcui": ["403853", "403854", "403855"], "spl_set_id": ["017bc6a3-5b3d-2381-e063-6394a90abece"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["AvKARE"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (42291-925-90)", "package_ndc": "42291-925-90", "marketing_start_date": "20230727"}], "brand_name": "olmesartan medoxomil-hydrochlorothiazide", "product_id": "42291-925_48bfa982-5678-139d-e063-6294a90adbfa", "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": "42291-925", "generic_name": "olmesartan medoxomil-hydrochlorothiazide", "labeler_name": "AvKARE", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "olmesartan medoxomil-hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "12.5 mg/1"}, {"name": "OLMESARTAN MEDOXOMIL", "strength": "40 mg/1"}], "application_number": "NDA021532", "marketing_category": "NDA", "marketing_start_date": "20230727", "listing_expiration_date": "20271231"}