Package 31722-886-32

{"route": ["ORAL"], "spl_id": "3d401487-0f8f-9ee8-e063-6394a90ac68d", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0331722888301", "0331722886307", "0331722887304"], "unii": ["0J48LPH2TH", "6M97XTV3HD"], "rxcui": ["403853", "403854", "403855"], "spl_set_id": ["d421f352-9500-4d3e-8bc3-0cdcc2050514"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Camber Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (31722-886-30)", "package_ndc": "31722-886-30", "marketing_start_date": "20250725"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (31722-886-32)  / 10 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "31722-886-32", "marketing_start_date": "20250725"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (31722-886-90)", "package_ndc": "31722-886-90", "marketing_start_date": "20250725"}], "brand_name": "Olmesartan medoxomil and hydrochlorothiazide", "product_id": "31722-886_3d401487-0f8f-9ee8-e063-6394a90ac68d", "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": "31722-886", "generic_name": "Olmesartan medoxomil and hydrochlorothiazide", "labeler_name": "Camber Pharmaceuticals, Inc.", "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": "ANDA209199", "marketing_category": "ANDA", "marketing_start_date": "20250725", "listing_expiration_date": "20261231"}