Package 71205-160-90

{"route": ["ORAL"], "spl_id": "982c815d-046b-47a5-abf7-f8a0c836543e", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["310434"], "spl_set_id": ["c09c66fd-cb31-41dd-b00b-acc58bd809f7"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71205-160-30)", "package_ndc": "71205-160-30", "marketing_start_date": "20181101"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71205-160-60)", "package_ndc": "71205-160-60", "marketing_start_date": "20181101"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (71205-160-90)", "package_ndc": "71205-160-90", "marketing_start_date": "20181101"}], "brand_name": "Gabapentin", "product_id": "71205-160_982c815d-046b-47a5-abf7-f8a0c836543e", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Anti-epileptic Agent [EPC]", "Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "71205-160", "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": "ANDA203244", "marketing_category": "ANDA", "marketing_start_date": "20140111", "listing_expiration_date": "20261231"}