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
76420-557-90	76420-557	HUMAN PRESCRIPTION DRUG	SPIRONOLACTONE	SPIRONOLACTONE	TABLET, FILM COATED	ORAL	20230407	N/A	ANDA	ANDA089424	Asclemed USA, Inc.	SPIRONOLACTONE	50 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (76420-557-90)
76420-558-01	76420-558	HUMAN PRESCRIPTION DRUG	SPIRONOLACTONE	SPIRONOLACTONE	TABLET, FILM COATED	ORAL	20230407	N/A	ANDA	ANDA089424	Asclemed USA, Inc.	SPIRONOLACTONE	100 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (76420-558-01)
76420-558-30	76420-558	HUMAN PRESCRIPTION DRUG	SPIRONOLACTONE	SPIRONOLACTONE	TABLET, FILM COATED	ORAL	20230407	N/A	ANDA	ANDA089424	Asclemed USA, Inc.	SPIRONOLACTONE	100 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (76420-558-30)
76420-558-60	76420-558	HUMAN PRESCRIPTION DRUG	SPIRONOLACTONE	SPIRONOLACTONE	TABLET, FILM COATED	ORAL	20230407	N/A	ANDA	ANDA089424	Asclemed USA, Inc.	SPIRONOLACTONE	100 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (76420-558-60)
76420-558-90	76420-558	HUMAN PRESCRIPTION DRUG	SPIRONOLACTONE	SPIRONOLACTONE	TABLET, FILM COATED	ORAL	20230407	N/A	ANDA	ANDA089424	Asclemed USA, Inc.	SPIRONOLACTONE	100 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (76420-558-90)