Package 71335-1965-1

{"route": ["ORAL"], "spl_id": "5f5bb283-9a75-49c5-8537-9cd1270c22ee", "openfda": {"nui": ["N0000175753", "N0000008486"], "unii": ["13AFD7670Q"], "rxcui": ["198150"], "spl_set_id": ["5067ff85-07f5-424c-b072-6907891e7b4e"], "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, PLASTIC (71335-1965-1)", "package_ndc": "71335-1965-1", "marketing_start_date": "20220503"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (71335-1965-2)", "package_ndc": "71335-1965-2", "marketing_start_date": "20211004"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE, PLASTIC (71335-1965-3)", "package_ndc": "71335-1965-3", "marketing_start_date": "20220503"}], "brand_name": "Primidone", "product_id": "71335-1965_5f5bb283-9a75-49c5-8537-9cd1270c22ee", "dosage_form": "TABLET", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "71335-1965", "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": "ANDA040586", "marketing_category": "ANDA", "marketing_start_date": "20210222", "listing_expiration_date": "20261231"}