Package 70518-2737-0

{"route": ["ORAL"], "spl_id": "4a8ce1d4-2226-613c-e063-6394a90ac366", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH", "3ST302B24A"], "rxcui": ["979471"], "spl_set_id": ["9f9cd7a7-be95-4ea8-8247-eb7ecbd36936"], "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": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2737-0)", "package_ndc": "70518-2737-0", "marketing_start_date": "20200512"}], "brand_name": "Losartan Potassium and Hydrochlorothiazide", "product_id": "70518-2737_4a8ce1d4-2226-613c-e063-6394a90ac366", "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": "70518-2737", "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": "25 mg/1"}, {"name": "LOSARTAN POTASSIUM", "strength": "100 mg/1"}], "application_number": "ANDA091629", "marketing_category": "ANDA", "marketing_start_date": "20200512", "listing_expiration_date": "20271231"}