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
70771-1864-6	70771-1864	HUMAN PRESCRIPTION DRUG	ivabradine	ivabradine	TABLET	ORAL	20240702	N/A	ANDA	ANDA213442	Zydus Lifesciences Limited	IVABRADINE HYDROCHLORIDE	7.5 mg/1	60 TABLET in 1 BOTTLE (70771-1864-6)
70771-1864-8	70771-1864	HUMAN PRESCRIPTION DRUG	ivabradine	ivabradine	TABLET	ORAL	20240702	N/A	ANDA	ANDA213442	Zydus Lifesciences Limited	IVABRADINE HYDROCHLORIDE	7.5 mg/1	180 TABLET in 1 BOTTLE (70771-1864-8)
70710-1471-6	70710-1471	HUMAN PRESCRIPTION DRUG	ivabradine	ivabradine	TABLET	ORAL	20240702	N/A	ANDA	ANDA213442	Zydus Pharmaceuticals USA Inc.	IVABRADINE HYDROCHLORIDE	5 mg/1	60 TABLET in 1 BOTTLE (70710-1471-6)
70710-1471-8	70710-1471	HUMAN PRESCRIPTION DRUG	ivabradine	ivabradine	TABLET	ORAL	20240702	N/A	ANDA	ANDA213442	Zydus Pharmaceuticals USA Inc.	IVABRADINE HYDROCHLORIDE	5 mg/1	180 TABLET in 1 BOTTLE (70710-1471-8)
70710-1472-6	70710-1472	HUMAN PRESCRIPTION DRUG	ivabradine	ivabradine	TABLET	ORAL	20240702	N/A	ANDA	ANDA213442	Zydus Pharmaceuticals USA Inc.	IVABRADINE HYDROCHLORIDE	7.5 mg/1	60 TABLET in 1 BOTTLE (70710-1472-6)
70710-1472-8	70710-1472	HUMAN PRESCRIPTION DRUG	ivabradine	ivabradine	TABLET	ORAL	20240702	N/A	ANDA	ANDA213442	Zydus Pharmaceuticals USA Inc.	IVABRADINE HYDROCHLORIDE	7.5 mg/1	180 TABLET in 1 BOTTLE (70710-1472-8)
70771-1863-6	70771-1863	HUMAN PRESCRIPTION DRUG	ivabradine	ivabradine	TABLET	ORAL	20240702	N/A	ANDA	ANDA213442	Zydus Lifesciences Limited	IVABRADINE HYDROCHLORIDE	5 mg/1	60 TABLET in 1 BOTTLE (70771-1863-6)
70771-1863-8	70771-1863	HUMAN PRESCRIPTION DRUG	ivabradine	ivabradine	TABLET	ORAL	20240702	N/A	ANDA	ANDA213442	Zydus Lifesciences Limited	IVABRADINE HYDROCHLORIDE	5 mg/1	180 TABLET in 1 BOTTLE (70771-1863-8)