Package 63629-7811-3

{"route": ["ORAL"], "spl_id": "53cadff5-416c-4786-aafe-edf62e11941a", "openfda": {"nui": ["N0000175753", "N0000008486"], "unii": ["13AFD7670Q"], "rxcui": ["198150"], "spl_set_id": ["93b4b34c-6dba-4aec-b98e-b2b18feb86a9"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "pharm_class_epc": ["Anti-epileptic Agent [EPC]"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (63629-7811-1)", "package_ndc": "63629-7811-1", "marketing_start_date": "20181023"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (63629-7811-2)", "package_ndc": "63629-7811-2", "marketing_start_date": "20190319"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (63629-7811-3)", "package_ndc": "63629-7811-3", "marketing_start_date": "20240403"}], "brand_name": "Primidone", "product_id": "63629-7811_53cadff5-416c-4786-aafe-edf62e11941a", "dosage_form": "TABLET", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "63629-7811", "generic_name": "Primidone", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Primidone", "active_ingredients": [{"name": "PRIMIDONE", "strength": "50 mg/1"}], "application_number": "ANDA040866", "marketing_category": "ANDA", "marketing_start_date": "20091224", "listing_expiration_date": "20261231"}