Package 50090-4993-0

{"route": ["ORAL"], "spl_id": "e1bcdea3-57f6-4e3c-aadc-a9204dff2f9e", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH", "3ST302B24A"], "rxcui": ["979471"], "spl_set_id": ["8a3e5be8-0a4b-48a0-817f-6e3c7674109d"], "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": "30 TABLET in 1 BOTTLE (50090-4993-0)", "package_ndc": "50090-4993-0", "marketing_start_date": "20200406"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (50090-4993-1)", "package_ndc": "50090-4993-1", "marketing_start_date": "20200406"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (50090-4993-2)", "package_ndc": "50090-4993-2", "marketing_start_date": "20250930"}], "brand_name": "Losartan Potassium and Hydrochlorothiazide", "product_id": "50090-4993_e1bcdea3-57f6-4e3c-aadc-a9204dff2f9e", "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": "50090-4993", "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": "25 mg/1"}, {"name": "LOSARTAN POTASSIUM", "strength": "100 mg/1"}], "application_number": "ANDA078245", "marketing_category": "ANDA", "marketing_start_date": "20101006", "listing_expiration_date": "20261231"}