Package 16571-117-50

{"route": ["ORAL"], "spl_id": "20c65bad-52d5-462e-aa17-5b7320f92b76", "openfda": {"nui": ["N0000008486"], "unii": ["6CW7F3G59X"], "rxcui": ["310433", "310434"], "spl_set_id": ["b1a9808d-31a5-4b63-afd0-d96d5a0ad7a1"], "pharm_class_pe": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (16571-117-01)", "package_ndc": "16571-117-01", "marketing_start_date": "20230719"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (16571-117-50)", "package_ndc": "16571-117-50", "marketing_start_date": "20230719"}], "brand_name": "Gabapentin", "product_id": "16571-117_20c65bad-52d5-462e-aa17-5b7320f92b76", "dosage_form": "TABLET", "pharm_class": ["Decreased Central Nervous System Disorganized Electrical Activity [PE]"], "product_ndc": "16571-117", "generic_name": "Gabapentin", "labeler_name": "Rising Pharma Holdings, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Gabapentin", "active_ingredients": [{"name": "GABAPENTIN", "strength": "800 mg/1"}], "application_number": "ANDA217995", "marketing_category": "ANDA", "marketing_start_date": "20230719", "listing_expiration_date": "20261231"}