Package 71205-411-30

{"route": ["ORAL"], "spl_id": "0f92415d-6d81-4cc1-9a3b-028430951eb8", "openfda": {"nui": ["N0000175753", "N0000008486"], "unii": ["VZI5B1W380"], "rxcui": ["312136"], "spl_set_id": ["95867dcd-fd0e-4570-987b-d35939f7d7d1"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "pharm_class_epc": ["Anti-epileptic Agent [EPC]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71205-411-30)", "package_ndc": "71205-411-30", "marketing_start_date": "20200226"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71205-411-60)", "package_ndc": "71205-411-60", "marketing_start_date": "20200226"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71205-411-90)", "package_ndc": "71205-411-90", "marketing_start_date": "20200226"}], "brand_name": "Oxcarbazepine", "product_id": "71205-411_0f92415d-6d81-4cc1-9a3b-028430951eb8", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "71205-411", "generic_name": "Oxcarbazepine", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Oxcarbazepine", "active_ingredients": [{"name": "OXCARBAZEPINE", "strength": "150 mg/1"}], "application_number": "ANDA077802", "marketing_category": "ANDA", "marketing_start_date": "20071009", "listing_expiration_date": "20261231"}