Package 71335-2617-2

{"route": ["ORAL"], "spl_id": "89dc73d5-773d-41a1-8fcc-77386ffec68e", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776", "N0000000070", "N0000175561"], "unii": ["0J48LPH2TH", "80M03YXJ7I"], "rxcui": ["200285"], "spl_set_id": ["d55b2f01-5cd1-40bb-8d36-34b5b9081ddc"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]", "Angiotensin 2 Receptor Blocker [EPC]"], "pharm_class_moa": ["Angiotensin 2 Receptor Antagonists [MoA]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71335-2617-1)", "package_ndc": "71335-2617-1", "marketing_start_date": "20250529"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71335-2617-2)", "package_ndc": "71335-2617-2", "marketing_start_date": "20250529"}], "brand_name": "VALSARTAN AND HYDROCHLOROTHIAZIDE", "product_id": "71335-2617_89dc73d5-773d-41a1-8fcc-77386ffec68e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]", "Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "71335-2617", "generic_name": "valsartan and hydrochlorothiazide", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "VALSARTAN AND HYDROCHLOROTHIAZIDE", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "12.5 mg/1"}, {"name": "VALSARTAN", "strength": "160 mg/1"}], "application_number": "ANDA206083", "marketing_category": "ANDA", "marketing_start_date": "20151031", "listing_expiration_date": "20261231"}