Package 72789-178-30

{"route": ["ORAL"], "spl_id": "373a4c73-f3c2-2c93-e063-6294a90ad5eb", "openfda": {"nui": ["N0000175753", "N0000008486"], "upc": ["0372789178301", "0372789177014"], "unii": ["13AFD7670Q"], "rxcui": ["96304", "198150"], "spl_set_id": ["0193c0a4-f593-609c-e063-6294a90aaa68"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "pharm_class_epc": ["Anti-epileptic Agent [EPC]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (72789-178-30)", "package_ndc": "72789-178-30", "marketing_start_date": "20230728"}], "brand_name": "Primidone", "product_id": "72789-178_373a4c73-f3c2-2c93-e063-6294a90ad5eb", "dosage_form": "TABLET", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "72789-178", "generic_name": "Primidone", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "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"}