Package 71205-774-30

{"route": ["ORAL"], "spl_id": "35004f84-90ae-45f0-a2ba-653dec507229", "openfda": {"nui": ["N0000008486"], "upc": ["0371205774905"], "unii": ["6CW7F3G59X"], "rxcui": ["310434"], "spl_set_id": ["35004f84-90ae-45f0-a2ba-653dec507229"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71205-774-30)", "package_ndc": "71205-774-30", "marketing_start_date": "20230314"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71205-774-60)", "package_ndc": "71205-774-60", "marketing_start_date": "20230314"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (71205-774-90)", "package_ndc": "71205-774-90", "marketing_start_date": "20230314"}], "brand_name": "Gabapentin", "product_id": "71205-774_35004f84-90ae-45f0-a2ba-653dec507229", "dosage_form": "TABLET", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "71205-774", "generic_name": "Gabapentin", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "800 mg/1"}], "application_number": "ANDA205101", "marketing_category": "ANDA", "marketing_start_date": "20160411", "listing_expiration_date": "20261231"}