Package 71610-671-45

{"route": ["ORAL"], "spl_id": "2d778122-9382-4e15-a927-d652112b3606", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH", "3ST302B24A"], "rxcui": ["979471"], "spl_set_id": ["35099fd1-1bc9-428b-9b9c-71f574cc4156"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-671-30)", "package_ndc": "71610-671-30", "marketing_start_date": "20221102"}, {"sample": false, "description": "45 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-671-45)", "package_ndc": "71610-671-45", "marketing_start_date": "20221102"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-671-53)", "package_ndc": "71610-671-53", "marketing_start_date": "20221103"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-671-60)", "package_ndc": "71610-671-60", "marketing_start_date": "20221102"}, {"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-671-70)", "package_ndc": "71610-671-70", "marketing_start_date": "20221102"}, {"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-671-80)", "package_ndc": "71610-671-80", "marketing_start_date": "20221102"}], "brand_name": "losartan potassium and hydrochlorothiazide", "product_id": "71610-671_2d778122-9382-4e15-a927-d652112b3606", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]", "Increased Diuresis [PE]", "Thiazide Diuretic [EPC]", "Thiazides [CS]"], "product_ndc": "71610-671", "generic_name": "losartan potassium and hydrochlorothiazide", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "losartan potassium and hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "25 mg/1"}, {"name": "LOSARTAN POTASSIUM", "strength": "100 mg/1"}], "application_number": "ANDA204832", "marketing_category": "ANDA", "marketing_start_date": "20170721", "listing_expiration_date": "20261231"}