Package 42658-103-08

{"route": ["ORAL"], "spl_id": "32efe915-7ba2-fb36-e063-6394a90a72ce", "openfda": {"upc": ["0358623200315"], "unii": ["3ST302B24A"], "rxcui": ["979480", "979485", "979492"], "spl_set_id": ["9af29d03-7192-4585-8e5f-82474c190af7"], "manufacturer_name": ["Hisun Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (42658-103-01)", "package_ndc": "42658-103-01", "marketing_start_date": "20250101"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (42658-103-04)", "package_ndc": "42658-103-04", "marketing_start_date": "20250101"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (42658-103-08)", "package_ndc": "42658-103-08", "marketing_start_date": "20250101"}], "brand_name": "LOSARTAN POTASSIUM", "product_id": "42658-103_32efe915-7ba2-fb36-e063-6394a90a72ce", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "42658-103", "generic_name": "LOSARTAN POTASSIUM", "labeler_name": "Hisun Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LOSARTAN POTASSIUM", "active_ingredients": [{"name": "LOSARTAN POTASSIUM", "strength": "50 mg/1"}], "application_number": "ANDA204795", "marketing_category": "ANDA", "marketing_start_date": "20250101", "listing_expiration_date": "20261231"}