Package 69584-362-10

{"route": ["ORAL"], "spl_id": "a86b0c8b-1ae7-4bfc-a236-c3d7fdd8959c", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH"], "rxcui": ["197770", "310798"], "spl_set_id": ["afbb9a0e-c22f-4133-8015-b4b2ab4d32e6"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Oxford Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (69584-362-10)", "package_ndc": "69584-362-10", "marketing_start_date": "20200925"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (69584-362-90)", "package_ndc": "69584-362-90", "marketing_start_date": "20200925"}], "brand_name": "Hydrochlorothiazide", "product_id": "69584-362_a86b0c8b-1ae7-4bfc-a236-c3d7fdd8959c", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "69584-362", "generic_name": "Hydrochlorothiazide", "labeler_name": "Oxford Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "50 mg/1"}], "application_number": "ANDA087068", "marketing_category": "ANDA", "marketing_start_date": "20200925", "listing_expiration_date": "20261231"}