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
63304-191-30	63304-191	HUMAN PRESCRIPTION DRUG	Desvenlafaxine	Desvenlafaxine	TABLET, EXTENDED RELEASE	ORAL	20130305	N/A	NDA	NDA204150	Sun Pharmaceutical Industries, Inc.	DESVENLAFAXINE	50 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (63304-191-30)
63304-191-90	63304-191	HUMAN PRESCRIPTION DRUG	Desvenlafaxine	Desvenlafaxine	TABLET, EXTENDED RELEASE	ORAL	20130305	N/A	NDA	NDA204150	Sun Pharmaceutical Industries, Inc.	DESVENLAFAXINE	50 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (63304-191-90)
63304-192-30	63304-192	HUMAN PRESCRIPTION DRUG	Desvenlafaxine	Desvenlafaxine	TABLET, EXTENDED RELEASE	ORAL	20130305	N/A	NDA	NDA204150	Sun Pharmaceutical Industries, Inc.	DESVENLAFAXINE	100 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (63304-192-30)
63304-192-90	63304-192	HUMAN PRESCRIPTION DRUG	Desvenlafaxine	Desvenlafaxine	TABLET, EXTENDED RELEASE	ORAL	20130305	N/A	NDA	NDA204150	Sun Pharmaceutical Industries, Inc.	DESVENLAFAXINE	100 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (63304-192-90)
46708-152-30	46708-152	HUMAN PRESCRIPTION DRUG	Desvenlafaxine	Desvenlafaxine	TABLET, EXTENDED RELEASE	ORAL	20130305	N/A	NDA	NDA204150	Alembic Pharmaceuticals Limited	DESVENLAFAXINE	50 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (46708-152-30)
46708-152-90	46708-152	HUMAN PRESCRIPTION DRUG	Desvenlafaxine	Desvenlafaxine	TABLET, EXTENDED RELEASE	ORAL	20130305	N/A	NDA	NDA204150	Alembic Pharmaceuticals Limited	DESVENLAFAXINE	50 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (46708-152-90)
46708-153-30	46708-153	HUMAN PRESCRIPTION DRUG	Desvenlafaxine	Desvenlafaxine	TABLET, EXTENDED RELEASE	ORAL	20130305	N/A	NDA	NDA204150	Alembic Pharmaceuticals Limited	DESVENLAFAXINE	100 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (46708-153-30)
46708-153-90	46708-153	HUMAN PRESCRIPTION DRUG	Desvenlafaxine	Desvenlafaxine	TABLET, EXTENDED RELEASE	ORAL	20130305	N/A	NDA	NDA204150	Alembic Pharmaceuticals Limited	DESVENLAFAXINE	100 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (46708-153-90)