Package 62559-661-90

{"route": ["ORAL"], "spl_id": "f88f68dc-85bd-494d-b111-07701c619ea5", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "upc": ["0362559662901", "0362559661904", "0362559660907"], "unii": ["0J48LPH2TH", "R85M2X0D68"], "rxcui": ["578325", "578330", "802749"], "spl_set_id": ["bd8d318d-167a-4b26-935d-265dde3193de"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["ANI Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (62559-661-90)", "package_ndc": "62559-661-90", "marketing_start_date": "20180926"}], "brand_name": "Candesartan Cilexetil and Hydrochlorothiazide", "product_id": "62559-661_f88f68dc-85bd-494d-b111-07701c619ea5", "dosage_form": "TABLET", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]", "Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "62559-661", "generic_name": "Candesartan Cilexetil and Hydrochlorothiazide", "labeler_name": "ANI Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Candesartan Cilexetil and Hydrochlorothiazide", "active_ingredients": [{"name": "CANDESARTAN CILEXETIL", "strength": "32 mg/1"}, {"name": "HYDROCHLOROTHIAZIDE", "strength": "12.5 mg/1"}], "application_number": "NDA021093", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20180926", "listing_expiration_date": "20261231"}