美国药品NDC（国家药品编码）与药品说明书数据库（U.S. FDA National Drug Code DataBase）

NDC包装代码	产品NDC	产品类型	商品名	通用名	剂型	给药途径	上市日期	结束日期	市场类别	申请号	标签持有者	活性成分	规格	包装描述
65219-184-20	65219-184	HUMAN PRESCRIPTION DRUG	ketamine hydrochloride	ketamine hydrochloride	INJECTION	INTRAMUSCULAR; INTRAVENOUS	20230710	N/A	ANDA	ANDA215808	Fresenius Kabi USA, LLC	KETAMINE HYDROCHLORIDE	10 mg/mL	10 VIAL in 1 TRAY (65219-184-20) / 20 mL in 1 VIAL (65219-184-01)
65219-186-23	65219-186	HUMAN PRESCRIPTION DRUG	ketamine hydrochloride	ketamine hydrochloride	INJECTION	INTRAMUSCULAR; INTRAVENOUS	20250418	N/A	ANDA	ANDA215808	Fresenius Kabi USA, LLC	KETAMINE HYDROCHLORIDE	100 mg/mL	10 VIAL in 1 TRAY (65219-186-23) / 5 mL in 1 VIAL (65219-186-13)
65219-186-05	65219-186	HUMAN PRESCRIPTION DRUG	ketamine hydrochloride	ketamine hydrochloride	INJECTION	INTRAMUSCULAR; INTRAVENOUS	20250418	N/A	ANDA	ANDA215808	Fresenius Kabi USA, LLC	KETAMINE HYDROCHLORIDE	100 mg/mL	10 VIAL in 1 TRAY (65219-186-05) / 5 mL in 1 VIAL (65219-186-01)
65219-188-10	65219-188	HUMAN PRESCRIPTION DRUG	ketamine hydrochloride	ketamine hydrochloride	INJECTION	INTRAMUSCULAR; INTRAVENOUS	20230710	N/A	ANDA	ANDA215808	Fresenius Kabi USA, LLC	KETAMINE HYDROCHLORIDE	50 mg/mL	10 VIAL in 1 TRAY (65219-188-10) / 10 mL in 1 VIAL (65219-188-01)