Package 50090-7768-0

{"route": ["ORAL"], "spl_id": "7ae37a19-2a35-4bfd-92f2-4a982a5d1023", "openfda": {"nui": ["N0000008486"], "unii": ["44YRR34555"], "rxcui": ["311289"], "spl_set_id": ["5eb7bea5-c95f-4a38-a5bb-c20d1549c797"], "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 (50090-7768-0)", "package_ndc": "50090-7768-0", "marketing_start_date": "20251117"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (50090-7768-1)", "package_ndc": "50090-7768-1", "marketing_start_date": "20251117"}], "brand_name": "Levetiracetam", "product_id": "50090-7768_7ae37a19-2a35-4bfd-92f2-4a982a5d1023", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "50090-7768", "generic_name": "Levetiracetam", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levetiracetam", "active_ingredients": [{"name": "LEVETIRACETAM", "strength": "500 mg/1"}], "application_number": "ANDA078993", "marketing_category": "ANDA", "marketing_start_date": "20090115", "listing_expiration_date": "20261231"}