Package 71335-0356-3

{"route": ["ORAL"], "spl_id": "d129026a-42e1-4532-b5f2-5ffcb783e3bd", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776", "N0000008859", "N0000175418"], "unii": ["0J48LPH2TH", "WS821Z52LQ"], "rxcui": ["310812"], "spl_set_id": ["ec6dce85-5c0b-475c-af0b-cbbc034f698f"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]", "Decreased Renal K+ Excretion [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]", "Potassium-sparing Diuretic [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-0356-1)", "package_ndc": "71335-0356-1", "marketing_start_date": "20180305"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-0356-2)", "package_ndc": "71335-0356-2", "marketing_start_date": "20180321"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-0356-3)", "package_ndc": "71335-0356-3", "marketing_start_date": "20241030"}], "brand_name": "Triamterene and Hydrochlorothiazide", "product_id": "71335-0356_d129026a-42e1-4532-b5f2-5ffcb783e3bd", "dosage_form": "TABLET", "pharm_class": ["Decreased Renal K+ Excretion [PE]", "Increased Diuresis [PE]", "Increased Diuresis [PE]", "Potassium-sparing Diuretic [EPC]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "71335-0356", "generic_name": "Triamterene and Hydrochlorothiazide", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Triamterene and Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "25 mg/1"}, {"name": "TRIAMTERENE", "strength": "37.5 mg/1"}], "application_number": "ANDA071251", "marketing_category": "ANDA", "marketing_start_date": "20090921", "listing_expiration_date": "20261231"}