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
47335-410-88	47335-410	HUMAN PRESCRIPTION DRUG	Sumatriptan and Naproxen Sodium	Sumatriptan and Naproxen Sodium	TABLET, FILM COATED	ORAL	20180720	N/A	ANDA	ANDA202803	Sun Pharmaceutical Industries, Inc.	NAPROXEN SODIUM; SUMATRIPTAN SUCCINATE	500 mg/1; 85 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (47335-410-88)
47335-410-83	47335-410	HUMAN PRESCRIPTION DRUG	Sumatriptan and Naproxen Sodium	Sumatriptan and Naproxen Sodium	TABLET, FILM COATED	ORAL	20180720	N/A	ANDA	ANDA202803	Sun Pharmaceutical Industries, Inc.	NAPROXEN SODIUM; SUMATRIPTAN SUCCINATE	500 mg/1; 85 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (47335-410-83)
47335-410-22	47335-410	HUMAN PRESCRIPTION DRUG	Sumatriptan and Naproxen Sodium	Sumatriptan and Naproxen Sodium	TABLET, FILM COATED	ORAL	20180720	N/A	ANDA	ANDA202803	Sun Pharmaceutical Industries, Inc.	NAPROXEN SODIUM; SUMATRIPTAN SUCCINATE	500 mg/1; 85 mg/1	9 TABLET, FILM COATED in 1 BOTTLE (47335-410-22)
16714-891-01	16714-891	HUMAN PRESCRIPTION DRUG	Sumatriptan and Naproxen Sodium	Sumatriptan and Naproxen Sodium	TABLET, FILM COATED	ORAL	20181127	N/A	ANDA	ANDA202803	NorthStar RxLLC	NAPROXEN SODIUM; SUMATRIPTAN SUCCINATE	500 mg/1; 85 mg/1	9 TABLET, FILM COATED in 1 BOTTLE (16714-891-01)