Package 68462-576-01

{"route": ["ORAL"], "spl_id": "51b0aed8-a229-4d2c-8fdf-aa957fddc41b", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0368462579015", "0368462576014", "0368462578018"], "unii": ["0J48LPH2TH", "N1SN99T69T"], "rxcui": ["898362", "898367", "898372", "898378"], "spl_set_id": ["51b0aed8-a229-4d2c-8fdf-aa957fddc41b"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Glenmark Pharmaceuticals Inc., USA"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (68462-576-01)", "package_ndc": "68462-576-01", "marketing_start_date": "20231201"}], "brand_name": "Benazepril Hydrochloride and Hydrochlorothiazide", "product_id": "68462-576_51b0aed8-a229-4d2c-8fdf-aa957fddc41b", "dosage_form": "TABLET, FILM COATED", "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": "68462-576", "generic_name": "Benazepril Hydrochloride and Hydrochlorothiazide", "labeler_name": "Glenmark Pharmaceuticals Inc., USA", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Benazepril Hydrochloride and Hydrochlorothiazide", "active_ingredients": [{"name": "BENAZEPRIL HYDROCHLORIDE", "strength": "5 mg/1"}, {"name": "HYDROCHLOROTHIAZIDE", "strength": "6.25 mg/1"}], "application_number": "ANDA076631", "marketing_category": "ANDA", "marketing_start_date": "20150317", "listing_expiration_date": "20261231"}