Package 50090-5962-1

{"route": ["ORAL"], "spl_id": "321701b0-f525-4704-ad7f-87c8bf8d01de", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH", "3ST302B24A"], "rxcui": ["979468"], "spl_set_id": ["a4aa7f77-c98d-4b70-84bb-e16a06fc7952"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-5962-0)", "package_ndc": "50090-5962-0", "marketing_start_date": "20220418"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-5962-1)", "package_ndc": "50090-5962-1", "marketing_start_date": "20220418"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (50090-5962-2)", "package_ndc": "50090-5962-2", "marketing_start_date": "20230313"}], "brand_name": "Losartan Potassium and Hydrochlorothiazide", "product_id": "50090-5962_321701b0-f525-4704-ad7f-87c8bf8d01de", "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": "50090-5962", "generic_name": "losartan potassium and hydrochlorothiazide", "labeler_name": "A-S Medication Solutions", "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": "ANDA201845", "marketing_category": "ANDA", "marketing_start_date": "20121030", "listing_expiration_date": "20261231"}