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
71209-028-05	71209-028	HUMAN PRESCRIPTION DRUG	VENLAFAXINE	venlafaxine	TABLET	ORAL	20181203	N/A	ANDA	ANDA206250	Cadila Pharmaceuticals Limited	VENLAFAXINE HYDROCHLORIDE	75 mg/1	100 TABLET in 1 BOTTLE (71209-028-05)
71209-027-05	71209-027	HUMAN PRESCRIPTION DRUG	VENLAFAXINE	venlafaxine	TABLET	ORAL	20181203	N/A	ANDA	ANDA206250	Cadila Pharmaceuticals Limited	VENLAFAXINE HYDROCHLORIDE	50 mg/1	100 TABLET in 1 BOTTLE (71209-027-05)
71209-025-05	71209-025	HUMAN PRESCRIPTION DRUG	VENLAFAXINE	venlafaxine	TABLET	ORAL	20181203	N/A	ANDA	ANDA206250	Cadila Pharmaceuticals Limited	VENLAFAXINE HYDROCHLORIDE	25 mg/1	100 TABLET in 1 BOTTLE (71209-025-05)
71209-029-05	71209-029	HUMAN PRESCRIPTION DRUG	VENLAFAXINE	venlafaxine	TABLET	ORAL	20181203	N/A	ANDA	ANDA206250	Cadila Pharmaceuticals Limited	VENLAFAXINE HYDROCHLORIDE	100 mg/1	100 TABLET in 1 BOTTLE (71209-029-05)
71209-026-05	71209-026	HUMAN PRESCRIPTION DRUG	VENLAFAXINE	venlafaxine	TABLET	ORAL	20181203	N/A	ANDA	ANDA206250	Cadila Pharmaceuticals Limited	VENLAFAXINE HYDROCHLORIDE	37.5 mg/1	100 TABLET in 1 BOTTLE (71209-026-05)