Package 68788-8367-6

{"route": ["ORAL"], "spl_id": "1ba78592-5daf-4d80-ae65-c71d84b7a06e", "openfda": {"unii": ["9N7R477WCK"], "rxcui": ["833709"], "spl_set_id": ["c30f6e9e-8014-40fc-9615-a6b8654137c1"], "manufacturer_name": ["Preferred Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "20 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8367-2)", "package_ndc": "68788-8367-2", "marketing_start_date": "20230201"}, {"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8367-3)", "package_ndc": "68788-8367-3", "marketing_start_date": "20230201"}, {"sample": false, "description": "60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8367-6)", "package_ndc": "68788-8367-6", "marketing_start_date": "20230201"}, {"sample": false, "description": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-8367-9)", "package_ndc": "68788-8367-9", "marketing_start_date": "20230201"}], "brand_name": "TRAMADOL HYDROCHLORIDE", "product_id": "68788-8367_1ba78592-5daf-4d80-ae65-c71d84b7a06e", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "68788-8367", "dea_schedule": "CIV", "generic_name": "TRAMADOL HYDROCHLORIDE", "labeler_name": "Preferred Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "TRAMADOL HYDROCHLORIDE", "active_ingredients": [{"name": "TRAMADOL HYDROCHLORIDE", "strength": "100 mg/1"}], "application_number": "ANDA200503", "marketing_category": "ANDA", "marketing_start_date": "20230201", "listing_expiration_date": "20261231"}