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
59762-0405-4	59762-0405	HUMAN PRESCRIPTION DRUG	Risedronate Sodium	Risedronate Sodium	TABLET, FILM COATED	ORAL	20020517	N/A	NDA AUTHORIZED GENERIC	NDA020835	Greenstone LLC	RISEDRONATE SODIUM HEMI-PENTAHYDRATE; RISEDRONATE SODIUM MONOHYDRATE	30.1 mg/1; 4.9 mg/1	4 TABLET, FILM COATED in 1 DOSE PACK (59762-0405-4)
59762-0405-5	59762-0405	HUMAN PRESCRIPTION DRUG	Risedronate Sodium	Risedronate Sodium	TABLET, FILM COATED	ORAL	20020517	20251130	NDA AUTHORIZED GENERIC	NDA020835	Greenstone LLC	RISEDRONATE SODIUM HEMI-PENTAHYDRATE; RISEDRONATE SODIUM MONOHYDRATE	30.1 mg/1; 4.9 mg/1	12 TABLET, FILM COATED in 1 DOSE PACK (59762-0405-5)
59762-0406-1	59762-0406	HUMAN PRESCRIPTION DRUG	Risedronate Sodium	Risedronate Sodium	TABLET, FILM COATED	ORAL	20080422	N/A	NDA AUTHORIZED GENERIC	NDA020835	Greenstone LLC	RISEDRONATE SODIUM HEMI-PENTAHYDRATE; RISEDRONATE SODIUM MONOHYDRATE	129 mg/1; 21 mg/1	1 TABLET, FILM COATED in 1 DOSE PACK (59762-0406-1)
59762-0406-3	59762-0406	HUMAN PRESCRIPTION DRUG	Risedronate Sodium	Risedronate Sodium	TABLET, FILM COATED	ORAL	20080422	20251130	NDA AUTHORIZED GENERIC	NDA020835	Greenstone LLC	RISEDRONATE SODIUM HEMI-PENTAHYDRATE; RISEDRONATE SODIUM MONOHYDRATE	129 mg/1; 21 mg/1	3 TABLET, FILM COATED in 1 DOSE PACK (59762-0406-3)
0430-0472-03	0430-0472	HUMAN PRESCRIPTION DRUG	Actonel	Risedronate Sodium	TABLET, FILM COATED	ORAL	20020517	N/A	NDA	NDA020835	Allergan, Inc.	RISEDRONATE SODIUM HEMI-PENTAHYDRATE; RISEDRONATE SODIUM MONOHYDRATE	30.1 mg/1; 4.9 mg/1	4 TABLET, FILM COATED in 1 DOSE PACK (0430-0472-03)
0430-0472-07	0430-0472	HUMAN PRESCRIPTION DRUG	Actonel	Risedronate Sodium	TABLET, FILM COATED	ORAL	20020517	20251130	NDA	NDA020835	Allergan, Inc.	RISEDRONATE SODIUM HEMI-PENTAHYDRATE; RISEDRONATE SODIUM MONOHYDRATE	30.1 mg/1; 4.9 mg/1	12 TABLET, FILM COATED in 1 DOSE PACK (0430-0472-07)
0430-0478-01	0430-0478	HUMAN PRESCRIPTION DRUG	Actonel	Risedronate Sodium	TABLET, FILM COATED	ORAL	20080422	N/A	NDA	NDA020835	Allergan, Inc.	RISEDRONATE SODIUM HEMI-PENTAHYDRATE; RISEDRONATE SODIUM MONOHYDRATE	129 mg/1; 21 mg/1	1 TABLET, FILM COATED in 1 DOSE PACK (0430-0478-01)
0430-0478-02	0430-0478	HUMAN PRESCRIPTION DRUG	Actonel	Risedronate Sodium	TABLET, FILM COATED	ORAL	20080422	20251130	NDA	NDA020835	Allergan, Inc.	RISEDRONATE SODIUM HEMI-PENTAHYDRATE; RISEDRONATE SODIUM MONOHYDRATE	129 mg/1; 21 mg/1	3 TABLET, FILM COATED in 1 DOSE PACK (0430-0478-02)