Package 50268-686-15

{"route": ["ORAL"], "spl_id": "42dc4ff9-003f-d362-e063-6394a90ad6f9", "openfda": {"nui": ["N0000175753", "N0000008486"], "unii": ["13AFD7670Q"], "rxcui": ["96304", "198150"], "spl_set_id": ["a90d5ba6-4170-0b97-5ae3-fc707c9e4f1b"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "pharm_class_epc": ["Anti-epileptic Agent [EPC]"], "manufacturer_name": ["AvPAK"]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 BOX, UNIT-DOSE (50268-686-15)  / 1 TABLET in 1 BLISTER PACK (50268-686-11)", "package_ndc": "50268-686-15", "marketing_start_date": "20110519"}], "brand_name": "Primidone", "product_id": "50268-686_42dc4ff9-003f-d362-e063-6394a90ad6f9", "dosage_form": "TABLET", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "50268-686", "generic_name": "Primidone", "labeler_name": "AvPAK", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Primidone", "active_ingredients": [{"name": "PRIMIDONE", "strength": "50 mg/1"}], "application_number": "ANDA040866", "marketing_category": "ANDA", "marketing_start_date": "20110519", "listing_expiration_date": "20261231"}