Package 72789-178-82

{"route": ["ORAL"], "spl_id": "419df69c-92e1-79f5-e063-6294a90a3e68", "openfda": {"nui": ["N0000175753", "N0000008486"], "upc": ["0372789178820", "0372789177823"], "unii": ["13AFD7670Q"], "rxcui": ["96304", "198150"], "spl_set_id": ["6046e4e9-0c1e-4d1f-85fa-d2ce25c5dc34"], "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": "100 TABLET in 1 BOTTLE, PLASTIC (72789-178-01)", "package_ndc": "72789-178-01", "marketing_start_date": "20210330"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE, PLASTIC (72789-178-82)", "package_ndc": "72789-178-82", "marketing_start_date": "20210622"}], "brand_name": "Primidone", "product_id": "72789-178_419df69c-92e1-79f5-e063-6294a90a3e68", "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"}