Package 65862-161-90

{"route": ["ORAL"], "spl_id": "5842ecc2-874a-481b-8997-afa9d862dc5d", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0365862161901"], "unii": ["0J48LPH2TH", "33067B3N2M"], "rxcui": ["310796", "310797", "310809"], "spl_set_id": ["50a58159-9572-4445-9859-b392632597da"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (65862-161-90)", "package_ndc": "65862-161-90", "marketing_start_date": "20070824"}], "brand_name": "QUINAPRIL HYDROCHLORIDE/HYDROCHLOROTHIAZIDE", "product_id": "65862-161_5842ecc2-874a-481b-8997-afa9d862dc5d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin Converting Enzyme Inhibitor [EPC]", "Angiotensin-converting Enzyme Inhibitors [MoA]", "Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "65862-161", "generic_name": "QUINAPRIL HYDROCHLORIDE/HYDROCHLOROTHIAZIDE", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "QUINAPRIL HYDROCHLORIDE/HYDROCHLOROTHIAZIDE", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "12.5 mg/1"}, {"name": "QUINAPRIL HYDROCHLORIDE", "strength": "10 mg/1"}], "application_number": "ANDA078450", "marketing_category": "ANDA", "marketing_start_date": "20070824", "listing_expiration_date": "20261231"}