Package 70518-3404-0

{"route": ["ORAL"], "spl_id": "3a8653a9-11c6-f12a-e063-6294a90a09fc", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH", "3ST302B24A"], "rxcui": ["979468"], "spl_set_id": ["03c0ec8d-9daf-43e8-8a4e-a2ddc3573ca7"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3404-0)", "package_ndc": "70518-3404-0", "marketing_start_date": "20220407"}], "brand_name": "Losartan Potassium and Hydrochlorothiazide", "product_id": "70518-3404_3a8653a9-11c6-f12a-e063-6294a90a09fc", "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": "70518-3404", "generic_name": "losartan potassium and hydrochlorothiazide", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Losartan Potassium and Hydrochlorothiazide", "active_ingredients": [{"name": "HYDROCHLOROTHIAZIDE", "strength": "12.5 mg/1"}, {"name": "LOSARTAN POTASSIUM", "strength": "50 mg/1"}], "application_number": "ANDA204901", "marketing_category": "ANDA", "marketing_start_date": "20220407", "listing_expiration_date": "20261231"}