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
68083-504-10	68083-504	HUMAN PRESCRIPTION DRUG	Ketamine Hydrochloride	Ketamine Hydrochloride	INJECTION, SOLUTION	INTRAMUSCULAR; INTRAVENOUS	20230124	N/A	ANDA	ANDA216809	Gland Pharma Limited	KETAMINE HYDROCHLORIDE	10 mg/mL	10 VIAL in 1 CARTON (68083-504-10) / 20 mL in 1 VIAL
68083-505-10	68083-505	HUMAN PRESCRIPTION DRUG	Ketamine Hydrochloride	Ketamine Hydrochloride	INJECTION, SOLUTION	INTRAMUSCULAR; INTRAVENOUS	20230124	N/A	ANDA	ANDA216809	Gland Pharma Limited	KETAMINE HYDROCHLORIDE	50 mg/mL	10 VIAL in 1 CARTON (68083-505-10) / 10 mL in 1 VIAL
68083-506-10	68083-506	HUMAN PRESCRIPTION DRUG	Ketamine Hydrochloride	Ketamine Hydrochloride	INJECTION, SOLUTION	INTRAMUSCULAR; INTRAVENOUS	20230124	N/A	ANDA	ANDA216809	Gland Pharma Limited	KETAMINE HYDROCHLORIDE	100 mg/mL	10 VIAL in 1 CARTON (68083-506-10) / 5 mL in 1 VIAL
25021-682-20	25021-682	HUMAN PRESCRIPTION DRUG	Ketamine Hydrochloride	Ketamine Hydrochloride	INJECTION, SOLUTION	INTRAMUSCULAR; INTRAVENOUS	20230715	N/A	ANDA	ANDA216809	Sagent Pharmaceuticals	KETAMINE HYDROCHLORIDE	10 mg/mL	10 VIAL in 1 CARTON (25021-682-20) / 20 mL in 1 VIAL
25021-683-10	25021-683	HUMAN PRESCRIPTION DRUG	Ketamine Hydrochloride	Ketamine Hydrochloride	INJECTION, SOLUTION	INTRAMUSCULAR; INTRAVENOUS	20230715	N/A	ANDA	ANDA216809	Sagent Pharmaceuticals	KETAMINE HYDROCHLORIDE	50 mg/mL	10 VIAL in 1 CARTON (25021-683-10) / 10 mL in 1 VIAL
25021-684-05	25021-684	HUMAN PRESCRIPTION DRUG	Ketamine Hydrochloride	Ketamine Hydrochloride	INJECTION, SOLUTION	INTRAMUSCULAR; INTRAVENOUS	20230715	N/A	ANDA	ANDA216809	Sagent Pharmaceuticals	KETAMINE HYDROCHLORIDE	100 mg/mL	10 VIAL in 1 CARTON (25021-684-05) / 5 mL in 1 VIAL