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
68682-001-50	68682-001	HUMAN PRESCRIPTION DRUG	SODIUM PHENYLACETATE AND SODIUM BENZOATE	SODIUM PHENYLACETATE AND SODIUM BENZOATE	INJECTION, SOLUTION, CONCENTRATE	INTRAVENOUS	20170315	N/A	NDA AUTHORIZED GENERIC	NDA020645	Oceanside Pharmaceuticals	SODIUM BENZOATE; SODIUM PHENYLACETATE	100 mg/mL; 100 mg/mL	1 VIAL, SINGLE-USE in 1 CARTON (68682-001-50) / 50 mL in 1 VIAL, SINGLE-USE
0187-0010-50	0187-0010	HUMAN PRESCRIPTION DRUG	Ammonul	sodium phenylacetate and sodium benzoate	INJECTION, SOLUTION, CONCENTRATE	INTRAVENOUS	20050217	N/A	NDA	NDA020645	Bausch Health US LLC	SODIUM BENZOATE; SODIUM PHENYLACETATE	100 mg/mL; 100 mg/mL	1 VIAL, SINGLE-USE in 1 CARTON (0187-0010-50) / 50 mL in 1 VIAL, SINGLE-USE