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
71205-714-04	71205-714	HUMAN PRESCRIPTION DRUG	Risedronate Sodium	Risedronate Sodium	TABLET, FILM COATED	ORAL	20221110	N/A	ANDA	ANDA090877	Proficient Rx LP	RISEDRONATE SODIUM	35 mg/1	1 BLISTER PACK in 1 CARTON (71205-714-04) / 4 TABLET, FILM COATED in 1 BLISTER PACK
60505-3165-0	60505-3165	HUMAN PRESCRIPTION DRUG	Risedronate Sodium	Risedronate Sodium	TABLET, FILM COATED	ORAL	20151130	N/A	ANDA	ANDA090877	Apotex Corp.	RISEDRONATE SODIUM	35 mg/1	1 BLISTER PACK in 1 CARTON (60505-3165-0) / 4 TABLET, FILM COATED in 1 BLISTER PACK
60505-3165-2	60505-3165	HUMAN PRESCRIPTION DRUG	Risedronate Sodium	Risedronate Sodium	TABLET, FILM COATED	ORAL	20151130	N/A	ANDA	ANDA090877	Apotex Corp.	RISEDRONATE SODIUM	35 mg/1	3 BLISTER PACK in 1 CARTON (60505-3165-2) / 4 TABLET, FILM COATED in 1 BLISTER PACK
60505-3097-4	60505-3097	HUMAN PRESCRIPTION DRUG	Risedronate Sodium	Risedronate Sodium	TABLET, FILM COATED	ORAL	20140611	N/A	ANDA	ANDA090877	Apotex Corp.	RISEDRONATE SODIUM	150 mg/1	1 BLISTER PACK in 1 CARTON (60505-3097-4) / 3 TABLET, FILM COATED in 1 BLISTER PACK
60505-3097-2	60505-3097	HUMAN PRESCRIPTION DRUG	Risedronate Sodium	Risedronate Sodium	TABLET, FILM COATED	ORAL	20140611	N/A	ANDA	ANDA090877	Apotex Corp.	RISEDRONATE SODIUM	150 mg/1	1 BLISTER PACK in 1 CARTON (60505-3097-2) / 1 TABLET, FILM COATED in 1 BLISTER PACK
60505-3096-2	60505-3096	HUMAN PRESCRIPTION DRUG	Risedronate Sodium	Risedronate Sodium	TABLET, FILM COATED	ORAL	20140611	N/A	ANDA	ANDA090877	Apotex Corp.	RISEDRONATE SODIUM	75 mg/1	1 BLISTER PACK in 1 CARTON (60505-3096-2) / 2 TABLET, FILM COATED in 1 BLISTER PACK