Package 51672-4137-4

{"route": ["ORAL"], "spl_id": "559a39a2-ec8e-443b-9df0-4c909633981c", "openfda": {"nui": ["N0000008486"], "upc": ["0351672414160"], "unii": ["44YRR34555"], "rxcui": ["311288", "311289", "311290", "387003", "403884"], "spl_set_id": ["bf412e94-ca36-4da9-83d7-fb0f1323cf21"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Taro Pharmaceuticals U.S.A., Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (51672-4137-4)", "package_ndc": "51672-4137-4", "marketing_start_date": "20100201"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (51672-4137-6)", "package_ndc": "51672-4137-6", "marketing_start_date": "20100201"}, {"sample": false, "description": "750 TABLET, FILM COATED in 1 BOTTLE (51672-4137-8)", "package_ndc": "51672-4137-8", "marketing_start_date": "20100201"}], "brand_name": "Levetiracetam", "product_id": "51672-4137_559a39a2-ec8e-443b-9df0-4c909633981c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "51672-4137", "generic_name": "Levetiracetam", "labeler_name": "Taro Pharmaceuticals U.S.A., Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levetiracetam", "active_ingredients": [{"name": "LEVETIRACETAM", "strength": "1000 mg/1"}], "application_number": "ANDA078960", "marketing_category": "ANDA", "marketing_start_date": "20100201", "listing_expiration_date": "20261231"}