Package 50090-7333-2

{"route": ["ORAL"], "spl_id": "e912f362-a9eb-47aa-a9f5-261deee63d79", "openfda": {"nui": ["N0000008486"], "unii": ["44YRR34555"], "rxcui": ["387003"], "spl_set_id": ["8a8472dc-b97e-445d-bf51-b6e618cae1b6"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (50090-7333-1)", "package_ndc": "50090-7333-1", "marketing_start_date": "20241015"}, {"sample": false, "description": "180 TABLET, FILM COATED in 1 BOTTLE (50090-7333-2)", "package_ndc": "50090-7333-2", "marketing_start_date": "20241015"}], "brand_name": "Levetiracetam", "product_id": "50090-7333_e912f362-a9eb-47aa-a9f5-261deee63d79", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "50090-7333", "generic_name": "Levetiracetam", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levetiracetam", "active_ingredients": [{"name": "LEVETIRACETAM", "strength": "1000 mg/1"}], "application_number": "ANDA215069", "marketing_category": "ANDA", "marketing_start_date": "20210611", "listing_expiration_date": "20261231"}