Package 72888-045-05

{"route": ["ORAL"], "spl_id": "48453b30-812c-76c6-e063-6394a90ad9a0", "openfda": {"nui": ["N0000175753", "N0000008486"], "upc": ["0372888160016", "0372888046051", "0372888160009", "0372888046013", "0372888045054", "0372888160054", "0372888045016"], "unii": ["13AFD7670Q"], "rxcui": ["96304", "198150", "328176"], "spl_set_id": ["b3b94d2e-6a64-45b7-b0cb-0fde689240d8"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "pharm_class_epc": ["Anti-epileptic Agent [EPC]"], "manufacturer_name": ["Advagen Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72888-045-01)", "package_ndc": "72888-045-01", "marketing_start_date": "20220628"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (72888-045-05)", "package_ndc": "72888-045-05", "marketing_start_date": "20220628"}], "brand_name": "Primidone", "product_id": "72888-045_48453b30-812c-76c6-e063-6394a90ad9a0", "dosage_form": "TABLET", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "72888-045", "generic_name": "Primidone", "labeler_name": "Advagen Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Primidone", "active_ingredients": [{"name": "PRIMIDONE", "strength": "50 mg/1"}], "application_number": "ANDA214896", "marketing_category": "ANDA", "marketing_start_date": "20220628", "listing_expiration_date": "20271231"}