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
62332-680-45	62332-680	HUMAN PRESCRIPTION DRUG	Ivabradine	Ivabradine	TABLET, FILM COATED	ORAL	20241220	N/A	ANDA	ANDA215238	Alembic Pharmaceuticals Inc.	IVABRADINE HYDROCHLORIDE	7.5 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (62332-680-45)
62332-680-60	62332-680	HUMAN PRESCRIPTION DRUG	Ivabradine	Ivabradine	TABLET, FILM COATED	ORAL	20241220	N/A	ANDA	ANDA215238	Alembic Pharmaceuticals Inc.	IVABRADINE HYDROCHLORIDE	7.5 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (62332-680-60)
62332-679-45	62332-679	HUMAN PRESCRIPTION DRUG	Ivabradine	Ivabradine	TABLET, FILM COATED	ORAL	20241220	N/A	ANDA	ANDA215238	Alembic Pharmaceuticals Inc.	IVABRADINE HYDROCHLORIDE	5 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (62332-679-45)
62332-679-60	62332-679	HUMAN PRESCRIPTION DRUG	Ivabradine	Ivabradine	TABLET, FILM COATED	ORAL	20241220	N/A	ANDA	ANDA215238	Alembic Pharmaceuticals Inc.	IVABRADINE HYDROCHLORIDE	5 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (62332-679-60)
46708-679-45	46708-679	HUMAN PRESCRIPTION DRUG	Ivabradine	Ivabradine	TABLET, FILM COATED	ORAL	20241220	N/A	ANDA	ANDA215238	Alembic Pharmaceuticals Limited	IVABRADINE HYDROCHLORIDE	5 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (46708-679-45)
46708-679-60	46708-679	HUMAN PRESCRIPTION DRUG	Ivabradine	Ivabradine	TABLET, FILM COATED	ORAL	20241220	N/A	ANDA	ANDA215238	Alembic Pharmaceuticals Limited	IVABRADINE HYDROCHLORIDE	5 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (46708-679-60)
46708-680-45	46708-680	HUMAN PRESCRIPTION DRUG	Ivabradine	Ivabradine	TABLET, FILM COATED	ORAL	20241220	N/A	ANDA	ANDA215238	Alembic Pharmaceuticals Limited	IVABRADINE HYDROCHLORIDE	7.5 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (46708-680-45)
46708-680-60	46708-680	HUMAN PRESCRIPTION DRUG	Ivabradine	Ivabradine	TABLET, FILM COATED	ORAL	20241220	N/A	ANDA	ANDA215238	Alembic Pharmaceuticals Limited	IVABRADINE HYDROCHLORIDE	7.5 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (46708-680-60)