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
47335-666-08	47335-666	HUMAN PRESCRIPTION DRUG	risedronate sodium	risedronate sodium	TABLET, FILM COATED	ORAL	20151130	N/A	ANDA	ANDA090886	Sun Pharmaceutical Industries, Inc.	RISEDRONATE SODIUM HEMI-PENTAHYDRATE	5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (47335-666-08)
47335-666-18	47335-666	HUMAN PRESCRIPTION DRUG	risedronate sodium	risedronate sodium	TABLET, FILM COATED	ORAL	20151130	N/A	ANDA	ANDA090886	Sun Pharmaceutical Industries, Inc.	RISEDRONATE SODIUM HEMI-PENTAHYDRATE	5 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (47335-666-18)
47335-666-83	47335-666	HUMAN PRESCRIPTION DRUG	risedronate sodium	risedronate sodium	TABLET, FILM COATED	ORAL	20151130	N/A	ANDA	ANDA090886	Sun Pharmaceutical Industries, Inc.	RISEDRONATE SODIUM HEMI-PENTAHYDRATE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (47335-666-83)
47335-666-88	47335-666	HUMAN PRESCRIPTION DRUG	risedronate sodium	risedronate sodium	TABLET, FILM COATED	ORAL	20151130	N/A	ANDA	ANDA090886	Sun Pharmaceutical Industries, Inc.	RISEDRONATE SODIUM HEMI-PENTAHYDRATE	5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (47335-666-88)
47335-667-08	47335-667	HUMAN PRESCRIPTION DRUG	risedronate sodium	risedronate sodium	TABLET, FILM COATED	ORAL	20151130	N/A	ANDA	ANDA090886	Sun Pharmaceutical Industries, Inc.	RISEDRONATE SODIUM HEMI-PENTAHYDRATE	30 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (47335-667-08)
47335-667-18	47335-667	HUMAN PRESCRIPTION DRUG	risedronate sodium	risedronate sodium	TABLET, FILM COATED	ORAL	20151130	N/A	ANDA	ANDA090886	Sun Pharmaceutical Industries, Inc.	RISEDRONATE SODIUM HEMI-PENTAHYDRATE	30 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (47335-667-18)
47335-667-83	47335-667	HUMAN PRESCRIPTION DRUG	risedronate sodium	risedronate sodium	TABLET, FILM COATED	ORAL	20151130	N/A	ANDA	ANDA090886	Sun Pharmaceutical Industries, Inc.	RISEDRONATE SODIUM HEMI-PENTAHYDRATE	30 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (47335-667-83)
47335-667-88	47335-667	HUMAN PRESCRIPTION DRUG	risedronate sodium	risedronate sodium	TABLET, FILM COATED	ORAL	20151130	N/A	ANDA	ANDA090886	Sun Pharmaceutical Industries, Inc.	RISEDRONATE SODIUM HEMI-PENTAHYDRATE	30 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (47335-667-88)
47335-668-62	47335-668	HUMAN PRESCRIPTION DRUG	risedronate sodium	risedronate sodium	TABLET, FILM COATED	ORAL	20151130	N/A	ANDA	ANDA090886	Sun Pharmaceutical Industries, Inc.	RISEDRONATE SODIUM HEMI-PENTAHYDRATE	35 mg/1	3 BLISTER PACK in 1 CARTON (47335-668-62) / 4 TABLET, FILM COATED in 1 BLISTER PACK
47335-668-68	47335-668	HUMAN PRESCRIPTION DRUG	risedronate sodium	risedronate sodium	TABLET, FILM COATED	ORAL	20151130	N/A	ANDA	ANDA090886	Sun Pharmaceutical Industries, Inc.	RISEDRONATE SODIUM HEMI-PENTAHYDRATE	35 mg/1	1 BLISTER PACK in 1 CARTON (47335-668-68) / 4 TABLET, FILM COATED in 1 BLISTER PACK
47335-727-98	47335-727	HUMAN PRESCRIPTION DRUG	risedronate sodium	risedronate sodium	TABLET, FILM COATED	ORAL	20140611	N/A	ANDA	ANDA090886	Sun Pharmaceutical Industries, Inc.	RISEDRONATE SODIUM HEMI-PENTAHYDRATE	75 mg/1	1 BLISTER PACK in 1 CARTON (47335-727-98) / 2 TABLET, FILM COATED in 1 BLISTER PACK
47335-928-60	47335-928	HUMAN PRESCRIPTION DRUG	risedronate sodium	risedronate sodium	TABLET, FILM COATED	ORAL	20140611	N/A	ANDA	ANDA090886	Sun Pharmaceutical Industries, Inc.	RISEDRONATE SODIUM HEMI-PENTAHYDRATE	150 mg/1	1 BLISTER PACK in 1 CARTON (47335-928-60) / 1 TABLET, FILM COATED in 1 BLISTER PACK
47335-928-67	47335-928	HUMAN PRESCRIPTION DRUG	risedronate sodium	risedronate sodium	TABLET, FILM COATED	ORAL	20140611	N/A	ANDA	ANDA090886	Sun Pharmaceutical Industries, Inc.	RISEDRONATE SODIUM HEMI-PENTAHYDRATE	150 mg/1	3 BLISTER PACK in 1 CARTON (47335-928-67) / 1 TABLET, FILM COATED in 1 BLISTER PACK