Package 69584-685-50

{"route": ["ORAL"], "spl_id": "86b0848d-c247-4e50-bc01-dce7dc157605", "openfda": {"nui": ["N0000175753", "N0000008486"], "unii": ["13AFD7670Q"], "rxcui": ["96304", "198150"], "spl_set_id": ["439096a4-c5d5-4ad8-be9c-238973a3e290"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "pharm_class_epc": ["Anti-epileptic Agent [EPC]"], "manufacturer_name": ["Oxford Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE, PLASTIC (69584-685-10)", "package_ndc": "69584-685-10", "marketing_start_date": "20210222"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (69584-685-50)", "package_ndc": "69584-685-50", "marketing_start_date": "20210222"}], "brand_name": "Primidone", "product_id": "69584-685_86b0848d-c247-4e50-bc01-dce7dc157605", "dosage_form": "TABLET", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "69584-685", "generic_name": "Primidone", "labeler_name": "Oxford Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Primidone", "active_ingredients": [{"name": "PRIMIDONE", "strength": "250 mg/1"}], "application_number": "ANDA040586", "marketing_category": "ANDA", "marketing_start_date": "20210222", "listing_expiration_date": "20261231"}