Package 68788-8517-0

{"route": ["ORAL"], "spl_id": "3f1d986b-6972-4150-9e34-823b6c2b5bbd", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH"], "rxcui": ["310798"], "spl_set_id": ["99f45e08-897d-44dd-b48d-aa6d78981f0c"], "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 (68788-8517-0)", "package_ndc": "68788-8517-0", "marketing_start_date": "20230901"}, {"sample": false, "description": "15 TABLET in 1 BOTTLE (68788-8517-1)", "package_ndc": "68788-8517-1", "marketing_start_date": "20230901"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (68788-8517-3)", "package_ndc": "68788-8517-3", "marketing_start_date": "20230901"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (68788-8517-6)", "package_ndc": "68788-8517-6", "marketing_start_date": "20230901"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68788-8517-9)", "package_ndc": "68788-8517-9", "marketing_start_date": "20230901"}], "brand_name": "Hydrochlorothiazide", "product_id": "68788-8517_3f1d986b-6972-4150-9e34-823b6c2b5bbd", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "68788-8517", "generic_name": "Hydrochlorothiazide", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "25 mg/1"}], "application_number": "ANDA040907", "marketing_category": "ANDA", "marketing_start_date": "20230901", "listing_expiration_date": "20261231"}