Package 50090-7775-0

{"route": ["ORAL"], "spl_id": "209d3e24-7513-4cf2-a4c9-8cf503b5e9c5", "openfda": {"nui": ["N0000008486"], "unii": ["44YRR34555"], "rxcui": ["311290"], "spl_set_id": ["6e31e766-6504-4f20-8831-1953363cace0"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (50090-7775-0)", "package_ndc": "50090-7775-0", "marketing_start_date": "20251119"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (50090-7775-1)", "package_ndc": "50090-7775-1", "marketing_start_date": "20251119"}], "brand_name": "Levetiracetam", "product_id": "50090-7775_209d3e24-7513-4cf2-a4c9-8cf503b5e9c5", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "50090-7775", "generic_name": "Levetiracetam", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levetiracetam", "active_ingredients": [{"name": "LEVETIRACETAM", "strength": "750 mg/1"}], "application_number": "ANDA078993", "marketing_category": "ANDA", "marketing_start_date": "20090115", "listing_expiration_date": "20261231"}