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
70771-1312-7	70771-1312	HUMAN PRESCRIPTION DRUG	Desvenlafaxine	Desvenlafaxine	TABLET, EXTENDED RELEASE	ORAL	20180508	N/A	ANDA	ANDA204020	Zydus Lifesciences Limited	DESVENLAFAXINE	100 mg/1	14 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1312-7)
70771-1312-9	70771-1312	HUMAN PRESCRIPTION DRUG	Desvenlafaxine	Desvenlafaxine	TABLET, EXTENDED RELEASE	ORAL	20180508	N/A	ANDA	ANDA204020	Zydus Lifesciences Limited	DESVENLAFAXINE	100 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1312-9)
70771-1661-3	70771-1661	HUMAN PRESCRIPTION DRUG	Desvenlafaxine	Desvenlafaxine	TABLET, EXTENDED RELEASE	ORAL	20221130	N/A	ANDA	ANDA204020	Zydus Lifesciences Limited	DESVENLAFAXINE	25 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1661-3)
70771-1661-9	70771-1661	HUMAN PRESCRIPTION DRUG	Desvenlafaxine	Desvenlafaxine	TABLET, EXTENDED RELEASE	ORAL	20221130	N/A	ANDA	ANDA204020	Zydus Lifesciences Limited	DESVENLAFAXINE	25 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1661-9)
68382-105-06	68382-105	HUMAN PRESCRIPTION DRUG	Desvenlafaxine	Desvenlafaxine	TABLET, EXTENDED RELEASE	ORAL	20230103	N/A	ANDA	ANDA204020	Zydus Pharmaceuticals USA Inc.	DESVENLAFAXINE	25 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-105-06)
68382-105-16	68382-105	HUMAN PRESCRIPTION DRUG	Desvenlafaxine	Desvenlafaxine	TABLET, EXTENDED RELEASE	ORAL	20230103	N/A	ANDA	ANDA204020	Zydus Pharmaceuticals USA Inc.	DESVENLAFAXINE	25 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-105-16)