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
82868-024-30	82868-024	HUMAN PRESCRIPTION DRUG	Diltiazem Hydrochloride	Diltiazem Hydrochloride	TABLET	ORAL	20231103	N/A	ANDA	ANDA216521	Northwind Health Company, LLC	DILTIAZEM HYDROCHLORIDE	60 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (82868-024-30)
50228-484-01	50228-484	HUMAN PRESCRIPTION DRUG	Diltiazem Hydrochloride	Diltiazem Hydrochloride	TABLET	ORAL	20220926	N/A	ANDA	ANDA216521	ScieGen Pharmaceuticals, Inc	DILTIAZEM HYDROCHLORIDE	120 mg/1	100 TABLET in 1 BOTTLE (50228-484-01)
50228-484-05	50228-484	HUMAN PRESCRIPTION DRUG	Diltiazem Hydrochloride	Diltiazem Hydrochloride	TABLET	ORAL	20220926	N/A	ANDA	ANDA216521	ScieGen Pharmaceuticals, Inc	DILTIAZEM HYDROCHLORIDE	120 mg/1	500 TABLET in 1 BOTTLE (50228-484-05)
50228-484-30	50228-484	HUMAN PRESCRIPTION DRUG	Diltiazem Hydrochloride	Diltiazem Hydrochloride	TABLET	ORAL	20220926	N/A	ANDA	ANDA216521	ScieGen Pharmaceuticals, Inc	DILTIAZEM HYDROCHLORIDE	120 mg/1	30 TABLET in 1 BOTTLE (50228-484-30)