Package 71335-0595-1

{"route": ["ORAL"], "spl_id": "83e47e72-5cf3-4db5-902e-20d7d9595cb9", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["UR59KN573L", "0J48LPH2TH"], "rxcui": ["854919"], "spl_set_id": ["447c11b6-72fe-418e-a2db-5d90b5347796"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (71335-0595-1)", "package_ndc": "71335-0595-1", "marketing_start_date": "20180625"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (71335-0595-2)", "package_ndc": "71335-0595-2", "marketing_start_date": "20190319"}, {"sample": false, "description": "28 TABLET in 1 BOTTLE, PLASTIC (71335-0595-3)", "package_ndc": "71335-0595-3", "marketing_start_date": "20240523"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (71335-0595-4)", "package_ndc": "71335-0595-4", "marketing_start_date": "20230719"}], "brand_name": "bisoprolol fumarate and hydrochlorothiazide", "product_id": "71335-0595_83e47e72-5cf3-4db5-902e-20d7d9595cb9", "dosage_form": "TABLET", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "71335-0595", "generic_name": "bisoprolol fumarate and hydrochlorothiazide", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "bisoprolol fumarate and hydrochlorothiazide", "active_ingredients": [{"name": "BISOPROLOL FUMARATE", "strength": "5 mg/1"}, {"name": "HYDROCHLOROTHIAZIDE", "strength": "6.25 mg/1"}], "application_number": "ANDA079106", "marketing_category": "ANDA", "marketing_start_date": "20101012", "listing_expiration_date": "20261231"}