Package 80425-0097-3

{"route": ["ORAL"], "spl_id": "2a998d83-7bad-3f5e-e063-6294a90acd3d", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["310433"], "spl_set_id": ["b37b1dcc-c7e9-8845-e053-2995a90a089e"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Advanced Rx of Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (80425-0097-1)", "package_ndc": "80425-0097-1", "marketing_start_date": "20111006"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (80425-0097-2)", "package_ndc": "80425-0097-2", "marketing_start_date": "20111006"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (80425-0097-3)", "package_ndc": "80425-0097-3", "marketing_start_date": "20111006"}, {"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (80425-0097-4)", "package_ndc": "80425-0097-4", "marketing_start_date": "20111006"}], "brand_name": "Gabapentin", "product_id": "80425-0097_2a998d83-7bad-3f5e-e063-6294a90acd3d", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "80425-0097", "generic_name": "Gabapentin", "labeler_name": "Advanced Rx of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "600 mg/1"}], "application_number": "ANDA200651", "marketing_category": "ANDA", "marketing_start_date": "20111006", "listing_expiration_date": "20261231"}