Package 30698-454-01

{"route": ["ORAL"], "spl_id": "4b9222f7-7b31-4781-e063-6394a90ab188", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0330698452011", "0330698454015", "0330698453018"], "unii": ["0J48LPH2TH", "N1SN99T69T"], "rxcui": ["898362", "898366", "898367", "898371", "898372", "898376"], "spl_set_id": ["94c4536f-e28e-48b1-8336-b3939917e99d"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Validus Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (30698-454-01)", "package_ndc": "30698-454-01", "marketing_start_date": "19920530"}], "brand_name": "Lotensin HCT", "product_id": "30698-454_4b9222f7-7b31-4781-e063-6394a90ab188", "dosage_form": "TABLET", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Decreased Blood Pressure [PE]", "Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "30698-454", "generic_name": "benazepril hydrochloride and hydrochlorothiazide", "labeler_name": "Validus Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Lotensin HCT", "active_ingredients": [{"name": "BENAZEPRIL HYDROCHLORIDE", "strength": "20 mg/1"}, {"name": "HYDROCHLOROTHIAZIDE", "strength": "25 mg/1"}], "application_number": "NDA020033", "marketing_category": "NDA", "marketing_start_date": "19920530", "listing_expiration_date": "20271231"}