Package 50090-4712-0

{"route": ["ORAL"], "spl_id": "1fd5cd7c-9ae2-4c09-97fb-0c2708743423", "openfda": {"unii": ["3ST302B24A"], "rxcui": ["979480"], "spl_set_id": ["27e783ce-3353-448a-b0a3-c954dfd2e4c7"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-4712-0)", "package_ndc": "50090-4712-0", "marketing_start_date": "20191112"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-4712-1)", "package_ndc": "50090-4712-1", "marketing_start_date": "20191112"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (50090-4712-2)", "package_ndc": "50090-4712-2", "marketing_start_date": "20240805"}], "brand_name": "Losartan Potassium", "product_id": "50090-4712_1fd5cd7c-9ae2-4c09-97fb-0c2708743423", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "50090-4712", "generic_name": "Losartan Potassium", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Losartan Potassium", "active_ingredients": [{"name": "LOSARTAN POTASSIUM", "strength": "100 mg/1"}], "application_number": "ANDA203835", "marketing_category": "ANDA", "marketing_start_date": "20150819", "listing_expiration_date": "20261231"}