Package 68071-3177-3

{"route": ["ORAL"], "spl_id": "1da08d15-0879-0132-e063-6394a90af9f5", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0368071317794"], "unii": ["0J48LPH2TH", "E7199S1YWR"], "rxcui": ["197886"], "spl_set_id": ["4af326db-bf2d-5310-e054-00144ff88e88"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (68071-3177-3)", "package_ndc": "68071-3177-3", "marketing_start_date": "20170317"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (68071-3177-6)", "package_ndc": "68071-3177-6", "marketing_start_date": "20170317"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68071-3177-9)", "package_ndc": "68071-3177-9", "marketing_start_date": "20170317"}], "brand_name": "Lisinopril and Hydrochlorothiazide", "product_id": "68071-3177_1da08d15-0879-0132-e063-6394a90af9f5", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "68071-3177", "generic_name": "Lisinopril and Hydrochlorothiazide", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lisinopril and Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "12.5 mg/1"}, {"name": "LISINOPRIL", "strength": "20 mg/1"}], "application_number": "ANDA077912", "marketing_category": "ANDA", "marketing_start_date": "20060410", "listing_expiration_date": "20261231"}