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
50419-541-01	50419-541	HUMAN PRESCRIPTION DRUG	Kerendia	finerenone	TABLET, FILM COATED	ORAL	20210709	N/A	NDA	NDA215341	Bayer Healthcare Pharmaceuticals Inc.	FINERENONE	20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50419-541-01)
50419-541-02	50419-541	HUMAN PRESCRIPTION DRUG	Kerendia	finerenone	TABLET, FILM COATED	ORAL	20210709	N/A	NDA	NDA215341	Bayer Healthcare Pharmaceuticals Inc.	FINERENONE	20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50419-541-02)
50419-540-70	50419-540	HUMAN PRESCRIPTION DRUG	Kerendia	finerenone	TABLET, FILM COATED	ORAL	20210709	N/A	NDA	NDA215341	Bayer Healthcare Pharmaceuticals Inc.	FINERENONE	10 mg/1	7 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50419-540-70)
50419-540-02	50419-540	HUMAN PRESCRIPTION DRUG	Kerendia	finerenone	TABLET, FILM COATED	ORAL	20210709	N/A	NDA	NDA215341	Bayer Healthcare Pharmaceuticals Inc.	FINERENONE	10 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50419-540-02)
50419-540-01	50419-540	HUMAN PRESCRIPTION DRUG	Kerendia	finerenone	TABLET, FILM COATED	ORAL	20210709	N/A	NDA	NDA215341	Bayer Healthcare Pharmaceuticals Inc.	FINERENONE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50419-540-01)
50419-541-70	50419-541	HUMAN PRESCRIPTION DRUG	Kerendia	finerenone	TABLET, FILM COATED	ORAL	20210709	N/A	NDA	NDA215341	Bayer Healthcare Pharmaceuticals Inc.	FINERENONE	20 mg/1	7 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50419-541-70)