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
0093-3100-56	0093-3100	HUMAN PRESCRIPTION DRUG	Risedronate Sodium	Risedronate Sodium	TABLET, FILM COATED	ORAL	20150601	N/A	ANDA	ANDA077132	Teva Pharmaceuticals USA, Inc.	RISEDRONATE SODIUM MONOHYDRATE	30 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0093-3100-56)
0093-3099-56	0093-3099	HUMAN PRESCRIPTION DRUG	Risedronate Sodium	Risedronate Sodium	TABLET, FILM COATED	ORAL	20150601	N/A	ANDA	ANDA077132	Teva Pharmaceuticals USA, Inc.	RISEDRONATE SODIUM MONOHYDRATE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0093-3099-56)
0093-3098-44	0093-3098	HUMAN PRESCRIPTION DRUG	Risedronate Sodium	Risedronate Sodium	TABLET, FILM COATED	ORAL	20150601	N/A	ANDA	ANDA077132	Teva Pharmaceuticals USA, Inc.	RISEDRONATE SODIUM MONOHYDRATE	35 mg/1	4 BLISTER PACK in 1 CARTON (0093-3098-44) / 1 TABLET, FILM COATED in 1 BLISTER PACK (0093-3098-19)
0093-3098-29	0093-3098	HUMAN PRESCRIPTION DRUG	Risedronate Sodium	Risedronate Sodium	TABLET, FILM COATED	ORAL	20150601	N/A	ANDA	ANDA077132	Teva Pharmaceuticals USA, Inc.	RISEDRONATE SODIUM MONOHYDRATE	35 mg/1	12 BLISTER PACK in 1 CARTON (0093-3098-29) / 1 TABLET, FILM COATED in 1 BLISTER PACK (0093-3098-19)