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
70594-090-02	70594-090	HUMAN PRESCRIPTION DRUG	CEFEPIME HYDROCHLORIDE	CEFEPIME HYDROCHLORIDE	INJECTION, POWDER, FOR SOLUTION	INTRAMUSCULAR; INTRAVENOUS	20210110	20251231	ANDA	ANDA212721	Xellia Pharmaceuticals USA LLC	CEFEPIME HYDROCHLORIDE	2 g/1	10 VIAL in 1 CARTON (70594-090-02) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (70594-090-01)
70594-089-02	70594-089	HUMAN PRESCRIPTION DRUG	CEFEPIME HYDROCHLORIDE	CEFEPIME HYDROCHLORIDE	INJECTION, POWDER, FOR SOLUTION	INTRAMUSCULAR; INTRAVENOUS	20210110	20251231	ANDA	ANDA212721	Xellia Pharmaceuticals USA LLC	CEFEPIME HYDROCHLORIDE	1 g/1	10 VIAL in 1 CARTON (70594-089-02) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (70594-089-01)