Package 68788-8813-3

{"route": ["ORAL"], "spl_id": "93f6a018-8b3d-4f40-be25-902daec19aea", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH"], "rxcui": ["429503"], "spl_set_id": ["93f6a018-8b3d-4f40-be25-902daec19aea"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "7 TABLET in 1 BOTTLE, PLASTIC (68788-8813-1)", "package_ndc": "68788-8813-1", "marketing_start_date": "20250121"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (68788-8813-3)", "package_ndc": "68788-8813-3", "marketing_start_date": "20250121"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (68788-8813-6)", "package_ndc": "68788-8813-6", "marketing_start_date": "20250121"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (68788-8813-8)", "package_ndc": "68788-8813-8", "marketing_start_date": "20250121"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (68788-8813-9)", "package_ndc": "68788-8813-9", "marketing_start_date": "20250121"}], "brand_name": "HYDROCHLOROTHIAZIDE", "product_id": "68788-8813_93f6a018-8b3d-4f40-be25-902daec19aea", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "68788-8813", "generic_name": "HYDROCHLOROTHIAZIDE", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HYDROCHLOROTHIAZIDE", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "12.5 mg/1"}], "application_number": "ANDA040702", "marketing_category": "ANDA", "marketing_start_date": "20250121", "listing_expiration_date": "20261231"}