Package 70518-4359-1

{"route": ["ORAL"], "spl_id": "3ac07946-a8b5-4392-e063-6394a90a1f75", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH"], "rxcui": ["310798"], "spl_set_id": ["31a3d1cb-0f52-4818-965d-7584374bb23e"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "15 TABLET in 1 BOTTLE, PLASTIC (70518-4359-0)", "package_ndc": "70518-4359-0", "marketing_start_date": "20250616"}, {"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-4359-1)", "package_ndc": "70518-4359-1", "marketing_start_date": "20250707"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (70518-4359-2)", "package_ndc": "70518-4359-2", "marketing_start_date": "20250724"}], "brand_name": "HYDROCHLOROTHIAZIDE", "product_id": "70518-4359_3ac07946-a8b5-4392-e063-6394a90a1f75", "dosage_form": "TABLET", "pharm_class": ["Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "70518-4359", "generic_name": "hydrochlorothiazide", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HYDROCHLOROTHIAZIDE", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "25 mg/1"}], "application_number": "ANDA085182", "marketing_category": "ANDA", "marketing_start_date": "20250616", "listing_expiration_date": "20261231"}