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
70518-1326-3	70518-1326	HUMAN PRESCRIPTION DRUG	verapamil hydrochloride	verapamil hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20260513	N/A	ANDA	ANDA078906	REMEDYREPACK INC.	VERAPAMIL HYDROCHLORIDE	240 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-1326-3)
51655-956-26	51655-956	HUMAN PRESCRIPTION DRUG	verapamil hydrochloride	verapamil hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20230518	N/A	ANDA	ANDA078906	Northwind Health Company, LLC	VERAPAMIL HYDROCHLORIDE	240 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-956-26)
51655-956-52	51655-956	HUMAN PRESCRIPTION DRUG	verapamil hydrochloride	verapamil hydrochloride	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20140527	N/A	ANDA	ANDA078906	Northwind Health Company, LLC	VERAPAMIL HYDROCHLORIDE	240 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, DISPENSING (51655-956-52)