Package 66490-690-10

{"route": ["ORAL"], "spl_id": "9d9f03b1-4eb4-4ba5-a357-600e368802c6", "openfda": {"nui": ["N0000175753", "N0000008486"], "unii": ["13AFD7670Q"], "rxcui": ["96304", "198150", "201747", "207478"], "spl_set_id": ["af593171-dabb-4ea3-b44c-89ed457b2c46"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "pharm_class_epc": ["Anti-epileptic Agent [EPC]"], "manufacturer_name": ["Bausch Health US, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (66490-690-10)", "package_ndc": "66490-690-10", "marketing_start_date": "20090624"}], "brand_name": "Mysoline", "product_id": "66490-690_9d9f03b1-4eb4-4ba5-a357-600e368802c6", "dosage_form": "TABLET", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "66490-690", "generic_name": "Primidone", "labeler_name": "Bausch Health US, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Mysoline", "active_ingredients": [{"name": "PRIMIDONE", "strength": "50 mg/1"}], "application_number": "NDA009170", "marketing_category": "NDA", "marketing_start_date": "20090624", "listing_expiration_date": "20261231"}