Package 60760-572-90

{"route": ["ORAL"], "spl_id": "eac58460-f797-274d-e053-2995a90a4c15", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH", "3ST302B24A"], "rxcui": ["979471"], "spl_set_id": ["eac57b4c-e79b-8d35-e053-2a95a90a9d25"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["ST. MARY'S MEDICAL PARK PHARMACY"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-572-90)", "package_ndc": "60760-572-90", "marketing_start_date": "20220930"}], "brand_name": "Losartan Potassium and Hydrochlorothiazide", "product_id": "60760-572_eac58460-f797-274d-e053-2995a90a4c15", "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": "60760-572", "generic_name": "losartan potassium and hydrochlorothiazide", "labeler_name": "ST. MARY'S MEDICAL PARK PHARMACY", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Losartan Potassium and Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "25 mg/1"}, {"name": "LOSARTAN POTASSIUM", "strength": "100 mg/1"}], "application_number": "ANDA204901", "marketing_category": "ANDA", "marketing_start_date": "20220930", "listing_expiration_date": "20261231"}