Package 60219-2348-4

{"route": ["ORAL"], "spl_id": "b19b19c4-cb47-4cbc-a914-dc73d4b655fa", "openfda": {"unii": ["9N7R477WCK"], "rxcui": ["835603"], "spl_set_id": ["8ec4e4e5-a56e-4198-8428-6b770b9bf27d"], "manufacturer_name": ["Amneal Pharmaceuticals NY LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, COATED in 1 BOTTLE (60219-2348-1)", "package_ndc": "60219-2348-1", "marketing_start_date": "20230213"}, {"sample": false, "description": "10 TABLET, COATED in 1 BOTTLE (60219-2348-4)", "package_ndc": "60219-2348-4", "marketing_start_date": "20230213"}, {"sample": false, "description": "500 TABLET, COATED in 1 BOTTLE (60219-2348-5)", "package_ndc": "60219-2348-5", "marketing_start_date": "20230213"}, {"sample": false, "description": "1000 TABLET, COATED in 1 BOTTLE (60219-2348-7)", "package_ndc": "60219-2348-7", "marketing_start_date": "20230213"}], "brand_name": "Tramadol Hydrochloride", "product_id": "60219-2348_b19b19c4-cb47-4cbc-a914-dc73d4b655fa", "dosage_form": "TABLET, COATED", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "60219-2348", "dea_schedule": "CIV", "generic_name": "Tramadol Hydrochloride", "labeler_name": "Amneal Pharmaceuticals NY LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Tramadol Hydrochloride", "active_ingredients": [{"name": "TRAMADOL HYDROCHLORIDE", "strength": "50 mg/1"}], "application_number": "ANDA076003", "marketing_category": "ANDA", "marketing_start_date": "20230213", "listing_expiration_date": "20261231"}