Package 42291-502-90

{"route": ["ORAL"], "spl_id": "3d743217-99d1-2bbc-e063-6294a90a6adf", "openfda": {"nui": ["N0000175359", "N0000175419", "M0471776"], "unii": ["0J48LPH2TH", "3ST302B24A"], "rxcui": ["979464", "979468", "979471"], "spl_set_id": ["e78b2195-a2da-3d03-e053-2a95a90a7d56"], "pharm_class_cs": ["Thiazides [CS]"], "pharm_class_pe": ["Increased Diuresis [PE]"], "pharm_class_epc": ["Thiazide Diuretic [EPC]"], "manufacturer_name": ["AvKARE"]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (42291-502-10)", "package_ndc": "42291-502-10", "marketing_start_date": "20250121"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (42291-502-90)", "package_ndc": "42291-502-90", "marketing_start_date": "20220831"}], "brand_name": "Losartan Potassium and Hydrochlorothiazide", "product_id": "42291-502_3d743217-99d1-2bbc-e063-6294a90a6adf", "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": "42291-502", "generic_name": "losartan potassium and hydrochlorothiazide", "labeler_name": "AvKARE", "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": "20220831", "listing_expiration_date": "20261231"}