Package 80425-0036-1

{"route": ["ORAL"], "spl_id": "2a985a04-15d4-b8b6-e063-6394a90a4231", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["310434"], "spl_set_id": ["afa28969-91c8-83fd-e053-2a95a90a656b"], "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 (80425-0036-1)", "package_ndc": "80425-0036-1", "marketing_start_date": "20111006"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (80425-0036-2)", "package_ndc": "80425-0036-2", "marketing_start_date": "20111006"}], "brand_name": "Gabapentin", "product_id": "80425-0036_2a985a04-15d4-b8b6-e063-6394a90a4231", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "80425-0036", "generic_name": "Gabapentin", "labeler_name": "Advanced Rx of Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "800 mg/1"}], "application_number": "ANDA200651", "marketing_category": "ANDA", "marketing_start_date": "20111006", "listing_expiration_date": "20261231"}