Package 71093-112-04

{"route": ["ORAL"], "spl_id": "c5f1ec3b-405e-4128-882b-43559d5083e5", "openfda": {"nui": ["N0000008486"], "upc": ["0371093112056"], "unii": ["6CW7F3G59X"], "rxcui": ["310433", "310434"], "spl_set_id": ["d7646d5e-ca25-4ec5-9e4b-931edcb15a0e"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["ACI Healthcare USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (71093-112-04)", "package_ndc": "71093-112-04", "marketing_start_date": "20140111"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (71093-112-05)", "package_ndc": "71093-112-05", "marketing_start_date": "20140111"}], "brand_name": "Gabapentin", "product_id": "71093-112_c5f1ec3b-405e-4128-882b-43559d5083e5", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "71093-112", "generic_name": "GABAPENTIN", "labeler_name": "ACI Healthcare USA, Inc.", "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"}