Package 16729-368-15

{"route": ["ORAL"], "spl_id": "424dfa88-8ad1-1ec4-e063-6394a90a8dcf", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0316729368100", "0316729366106", "0316729367103"], "unii": ["0J48LPH2TH", "6M97XTV3HD"], "rxcui": ["403853", "403854", "403855"], "spl_set_id": ["d858a6de-dda5-4bcd-a255-5723d01d896f"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Accord Healthcare Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (16729-368-15)", "package_ndc": "16729-368-15", "marketing_start_date": "20200903"}], "brand_name": "OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE", "product_id": "16729-368_424dfa88-8ad1-1ec4-e063-6394a90a8dcf", "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": "16729-368", "generic_name": "OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE", "labeler_name": "Accord Healthcare Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "25 mg/1"}, {"name": "OLMESARTAN MEDOXOMIL", "strength": "40 mg/1"}], "application_number": "ANDA209281", "marketing_category": "ANDA", "marketing_start_date": "20200903", "listing_expiration_date": "20261231"}