Package 68788-7790-0

{"route": ["ORAL"], "spl_id": "4fc36bb6-717a-45a5-8964-70b4c8557242", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH"], "rxcui": ["197770"], "spl_set_id": ["5ab641d8-cd22-4368-8070-18487dd801eb"], "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": "100 TABLET in 1 BOTTLE (68788-7790-0)", "package_ndc": "68788-7790-0", "marketing_start_date": "20201021"}, {"sample": false, "description": "15 TABLET in 1 BOTTLE (68788-7790-1)", "package_ndc": "68788-7790-1", "marketing_start_date": "20201021"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-7790-3)", "package_ndc": "68788-7790-3", "marketing_start_date": "20201021"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (68788-7790-6)", "package_ndc": "68788-7790-6", "marketing_start_date": "20201021"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68788-7790-9)", "package_ndc": "68788-7790-9", "marketing_start_date": "20201021"}], "brand_name": "HYDROCHLOROTHIAZIDE", "product_id": "68788-7790_4fc36bb6-717a-45a5-8964-70b4c8557242", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "68788-7790", "generic_name": "hydrochlorothiazide", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HYDROCHLOROTHIAZIDE", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "50 mg/1"}], "application_number": "ANDA085182", "marketing_category": "ANDA", "marketing_start_date": "20201021", "listing_expiration_date": "20261231"}