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
70518-3256-0	70518-3256	HUMAN PRESCRIPTION DRUG	PROPOFOL	PROPOFOL	INJECTION, EMULSION	INTRAVENOUS	20211025	N/A	ANDA	ANDA074848	REMEDYREPACK INC.	PROPOFOL	10 mg/mL	10 VIAL, SINGLE-USE in 1 CARTON (70518-3256-0) / 20 mL in 1 VIAL, SINGLE-USE
0641-6194-10	0641-6194	HUMAN PRESCRIPTION DRUG	PROPOFOL	PROPOFOL	INJECTION, EMULSION	INTRAVENOUS	20200501	N/A	ANDA	ANDA074848	Hikma Pharmaceuticals USA Inc.	PROPOFOL	10 mg/mL	10 VIAL, SINGLE-USE in 1 CARTON (0641-6194-10) / 20 mL in 1 VIAL, SINGLE-USE (0641-6194-01)
0641-6195-20	0641-6195	HUMAN PRESCRIPTION DRUG	PROPOFOL	PROPOFOL	INJECTION, EMULSION	INTRAVENOUS	20200501	N/A	ANDA	ANDA074848	Hikma Pharmaceuticals USA Inc.	PROPOFOL	10 mg/mL	20 VIAL, SINGLE-USE in 1 CARTON (0641-6195-20) / 50 mL in 1 VIAL, SINGLE-USE (0641-6195-01)
0641-6196-10	0641-6196	HUMAN PRESCRIPTION DRUG	PROPOFOL	PROPOFOL	INJECTION, EMULSION	INTRAVENOUS	20200501	N/A	ANDA	ANDA074848	Hikma Pharmaceuticals USA Inc.	PROPOFOL	10 mg/mL	10 VIAL, SINGLE-USE in 1 CARTON (0641-6196-10) / 100 mL in 1 VIAL, SINGLE-USE (0641-6196-01)