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
69238-2080-1	69238-2080	HUMAN PRESCRIPTION DRUG	Propranolol Hydrochloride	Propranolol Hydrochloride	TABLET	ORAL	20210603	N/A	ANDA	ANDA071976	Amneal Pharmaceuticals NY LLC	PROPRANOLOL HYDROCHLORIDE	60 mg/1	100 TABLET in 1 BOTTLE (69238-2080-1)
69238-2081-1	69238-2081	HUMAN PRESCRIPTION DRUG	Propranolol Hydrochloride	Propranolol Hydrochloride	TABLET	ORAL	20210603	N/A	ANDA	ANDA071976	Amneal Pharmaceuticals NY LLC	PROPRANOLOL HYDROCHLORIDE	80 mg/1	100 TABLET in 1 BOTTLE (69238-2081-1)
69238-2081-5	69238-2081	HUMAN PRESCRIPTION DRUG	Propranolol Hydrochloride	Propranolol Hydrochloride	TABLET	ORAL	20210603	N/A	ANDA	ANDA071976	Amneal Pharmaceuticals NY LLC	PROPRANOLOL HYDROCHLORIDE	80 mg/1	500 TABLET in 1 BOTTLE (69238-2081-5)
67046-1582-3	67046-1582	HUMAN PRESCRIPTION DRUG	Propranolol Hydrochloride	Propranolol Hydrochloride	TABLET	ORAL	20250908	N/A	ANDA	ANDA071976	Coupler LLC	PROPRANOLOL HYDROCHLORIDE	60 mg/1	30 TABLET in 1 BLISTER PACK (67046-1582-3)