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
63323-125-94	63323-125	HUMAN PRESCRIPTION DRUG	GEMCITABINE	GEMCITABINE	INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION	INTRAVENOUS	20110726	N/A	ANDA	ANDA090799	Fresenius Kabi USA, LLC	GEMCITABINE HYDROCHLORIDE	1 g/25mL	1 VIAL, SINGLE-DOSE in 1 BOX (63323-125-94) / 25 mL in 1 VIAL, SINGLE-DOSE
63323-126-03	63323-126	HUMAN PRESCRIPTION DRUG	GEMCITABINE	GEMCITABINE	INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION	INTRAVENOUS	20110726	N/A	ANDA	ANDA090799	Fresenius Kabi USA, LLC	GEMCITABINE HYDROCHLORIDE	2 g/50mL	1 VIAL, SINGLE-DOSE in 1 BOX (63323-126-03) / 50 mL in 1 VIAL, SINGLE-DOSE
63323-125-53	63323-125	HUMAN PRESCRIPTION DRUG	GEMCITABINE	GEMCITABINE	INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION	INTRAVENOUS	20110726	N/A	ANDA	ANDA090799	Fresenius Kabi USA, LLC	GEMCITABINE HYDROCHLORIDE	1 g/25mL	1 VIAL, SINGLE-DOSE in 1 BOX (63323-125-53) / 25 mL in 1 VIAL, SINGLE-DOSE
63323-102-94	63323-102	HUMAN PRESCRIPTION DRUG	GEMCITABINE	GEMCITABINE	INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION	INTRAVENOUS	20110726	N/A	ANDA	ANDA090799	Fresenius Kabi USA, LLC	GEMCITABINE HYDROCHLORIDE	200 mg/5mL	1 VIAL, SINGLE-DOSE in 1 BOX (63323-102-94) / 5 mL in 1 VIAL, SINGLE-DOSE
63323-102-13	63323-102	HUMAN PRESCRIPTION DRUG	GEMCITABINE	GEMCITABINE	INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION	INTRAVENOUS	20110726	N/A	ANDA	ANDA090799	Fresenius Kabi USA, LLC	GEMCITABINE HYDROCHLORIDE	200 mg/5mL	1 VIAL, SINGLE-DOSE in 1 BOX (63323-102-13) / 5 mL in 1 VIAL, SINGLE-DOSE