Package 50090-4489-0

{"route": ["ORAL"], "spl_id": "9edec7d5-8354-46fb-837d-393ce6b7f2d8", "openfda": {"unii": ["3ST302B24A"], "rxcui": ["979492"], "spl_set_id": ["f29cc61a-afba-4ecb-8043-5f103872f1ae"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50090-4489-0)", "package_ndc": "50090-4489-0", "marketing_start_date": "20190829"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-4489-1)", "package_ndc": "50090-4489-1", "marketing_start_date": "20190829"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (50090-4489-2)", "package_ndc": "50090-4489-2", "marketing_start_date": "20230809"}], "brand_name": "Losartan Potassium", "product_id": "50090-4489_9edec7d5-8354-46fb-837d-393ce6b7f2d8", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Angiotensin 2 Receptor Antagonists [MoA]", "Angiotensin 2 Receptor Blocker [EPC]"], "product_ndc": "50090-4489", "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": "50 mg/1"}], "application_number": "ANDA203835", "marketing_category": "ANDA", "marketing_start_date": "20150819", "listing_expiration_date": "20271231"}