Package 62559-414-01

{"route": ["ORAL"], "spl_id": "052493c7-89a3-452e-8140-04dd95f0d9e2", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0362559415019", "0362559416016", "0362559414012", "0362559417013"], "unii": ["0J48LPH2TH", "N1SN99T69T"], "rxcui": ["898362", "898367", "898372", "898378"], "spl_set_id": ["e6527adf-8c74-4d81-9199-d56a7fca895e"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["ANI Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (62559-414-01)", "package_ndc": "62559-414-01", "marketing_start_date": "20221107"}], "brand_name": "Benazepril Hydrochloride and Hydrochlorothiazide", "product_id": "62559-414_052493c7-89a3-452e-8140-04dd95f0d9e2", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]", "Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "62559-414", "generic_name": "Benazepril Hydrochloride and Hydrochlorothiazide", "labeler_name": "ANI Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Benazepril Hydrochloride and Hydrochlorothiazide", "active_ingredients": [{"name": "BENAZEPRIL HYDROCHLORIDE", "strength": "5 mg/1"}, {"name": "HYDROCHLOROTHIAZIDE", "strength": "6.25 mg/1"}], "application_number": "ANDA076342", "marketing_category": "ANDA", "marketing_start_date": "20221107", "listing_expiration_date": "20261231"}