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
82511-009-10	82511-009	HUMAN PRESCRIPTION DRUG	Gemcitabine hydrochloride	Gemcitabine hydrochloride	INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION	INTRAVENOUS	20240808	N/A	ANDA	ANDA078759	Teyro Labs Private Limited	GEMCITABINE HYDROCHLORIDE	1 g/25mL	1 VIAL, SINGLE-USE in 1 CARTON (82511-009-10) / 25 mL in 1 VIAL, SINGLE-USE
82511-008-20	82511-008	HUMAN PRESCRIPTION DRUG	Gemcitabine hydrochloride	Gemcitabine hydrochloride	INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION	INTRAVENOUS	20240808	N/A	ANDA	ANDA078759	Teyro Labs Private Limited	GEMCITABINE HYDROCHLORIDE	200 mg/5mL	1 VIAL, SINGLE-USE in 1 CARTON (82511-008-20) / 5 mL in 1 VIAL, SINGLE-USE