Package 81665-101-60

{"route": ["ORAL"], "spl_id": "c50830af-76fa-476a-a88d-50f38f9ecc42", "openfda": {"nui": ["N0000008486"], "unii": ["44YRR34555"], "rxcui": ["807832", "846378"], "spl_set_id": ["1a31134d-6b63-4d14-8445-0ed132e6c88d"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Omnivium Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "120 TABLET, EXTENDED RELEASE in 1 BOTTLE (81665-101-12)", "package_ndc": "81665-101-12", "marketing_start_date": "20230505"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (81665-101-60)", "package_ndc": "81665-101-60", "marketing_start_date": "20230505"}], "brand_name": "LEVETIRACETAM Extended-release", "product_id": "81665-101_c50830af-76fa-476a-a88d-50f38f9ecc42", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "81665-101", "generic_name": "LEVETIRACETAM", "labeler_name": "Omnivium Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "LEVETIRACETAM", "brand_name_suffix": "Extended-release", "active_ingredients": [{"name": "LEVETIRACETAM", "strength": "500 mg/1"}], "application_number": "ANDA212688", "marketing_category": "ANDA", "marketing_start_date": "20230505", "listing_expiration_date": "20271231"}