Package 59651-441-05

{"route": ["ORAL"], "spl_id": "7100e3d0-b751-47a1-a947-97c7573eec7a", "openfda": {"unii": ["9N7R477WCK"], "rxcui": ["835603"], "spl_set_id": ["e5005d9e-91cb-4ff8-bcf2-b5ee70cf4f3f"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (59651-441-01)", "package_ndc": "59651-441-01", "marketing_start_date": "20200923"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (59651-441-05)", "package_ndc": "59651-441-05", "marketing_start_date": "20200923"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (59651-441-99)", "package_ndc": "59651-441-99", "marketing_start_date": "20200923"}], "brand_name": "Tramadol Hydrochloride", "product_id": "59651-441_7100e3d0-b751-47a1-a947-97c7573eec7a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "59651-441", "dea_schedule": "CIV", "generic_name": "Tramadol Hydrochloride", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tramadol Hydrochloride", "active_ingredients": [{"name": "TRAMADOL HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA203494", "marketing_category": "ANDA", "marketing_start_date": "20200923", "listing_expiration_date": "20261231"}