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 Pharmaceuticals, LLC	DILTIAZEM HYDROCHLORIDE	60 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (82868-024-30)
82868-036-10	82868-036	HUMAN PRESCRIPTION DRUG	Diltiazem Hydrochloride	Diltiazem hydrochloride	TABLET	ORAL	20240118	N/A	ANDA	ANDA216521	Northwind Pharmaceuticals, LLC	DILTIAZEM HYDROCHLORIDE	30 mg/1	10 TABLET in 1 BOTTLE, PLASTIC (82868-036-10)
50228-481-01	50228-481	HUMAN PRESCRIPTION DRUG	Diltiazem Hydrochloride	Diltiazem hydrochloride	TABLET	ORAL	20220926	N/A	ANDA	ANDA216521	ScieGen Pharmaceuticals, Inc	DILTIAZEM HYDROCHLORIDE	30 mg/1	100 TABLET in 1 BOTTLE (50228-481-01)
50228-481-05	50228-481	HUMAN PRESCRIPTION DRUG	Diltiazem Hydrochloride	Diltiazem hydrochloride	TABLET	ORAL	20220926	N/A	ANDA	ANDA216521	ScieGen Pharmaceuticals, Inc	DILTIAZEM HYDROCHLORIDE	30 mg/1	500 TABLET in 1 BOTTLE (50228-481-05)
50228-481-10	50228-481	HUMAN PRESCRIPTION DRUG	Diltiazem Hydrochloride	Diltiazem hydrochloride	TABLET	ORAL	20220926	N/A	ANDA	ANDA216521	ScieGen Pharmaceuticals, Inc	DILTIAZEM HYDROCHLORIDE	30 mg/1	1000 TABLET in 1 BOTTLE (50228-481-10)
50228-481-30	50228-481	HUMAN PRESCRIPTION DRUG	Diltiazem Hydrochloride	Diltiazem hydrochloride	TABLET	ORAL	20220926	N/A	ANDA	ANDA216521	ScieGen Pharmaceuticals, Inc	DILTIAZEM HYDROCHLORIDE	30 mg/1	30 TABLET in 1 BOTTLE (50228-481-30)
50228-482-01	50228-482	HUMAN PRESCRIPTION DRUG	Diltiazem Hydrochloride	Diltiazem Hydrochloride	TABLET	ORAL	20220926	N/A	ANDA	ANDA216521	ScieGen Pharmaceuticals, Inc	DILTIAZEM HYDROCHLORIDE	60 mg/1	100 TABLET in 1 BOTTLE (50228-482-01)
50228-482-05	50228-482	HUMAN PRESCRIPTION DRUG	Diltiazem Hydrochloride	Diltiazem Hydrochloride	TABLET	ORAL	20220926	N/A	ANDA	ANDA216521	ScieGen Pharmaceuticals, Inc	DILTIAZEM HYDROCHLORIDE	60 mg/1	500 TABLET in 1 BOTTLE (50228-482-05)
50228-482-10	50228-482	HUMAN PRESCRIPTION DRUG	Diltiazem Hydrochloride	Diltiazem Hydrochloride	TABLET	ORAL	20220926	N/A	ANDA	ANDA216521	ScieGen Pharmaceuticals, Inc	DILTIAZEM HYDROCHLORIDE	60 mg/1	1000 TABLET in 1 BOTTLE (50228-482-10)
50228-482-30	50228-482	HUMAN PRESCRIPTION DRUG	Diltiazem Hydrochloride	Diltiazem Hydrochloride	TABLET	ORAL	20220926	N/A	ANDA	ANDA216521	ScieGen Pharmaceuticals, Inc	DILTIAZEM HYDROCHLORIDE	60 mg/1	30 TABLET in 1 BOTTLE (50228-482-30)
50228-483-01	50228-483	HUMAN PRESCRIPTION DRUG	Diltiazem Hydrochloride	Diltiazem Hydrochloride	TABLET	ORAL	20220926	N/A	ANDA	ANDA216521	ScieGen Pharmaceuticals, Inc	DILTIAZEM HYDROCHLORIDE	90 mg/1	100 TABLET in 1 BOTTLE (50228-483-01)
50228-483-05	50228-483	HUMAN PRESCRIPTION DRUG	Diltiazem Hydrochloride	Diltiazem Hydrochloride	TABLET	ORAL	20220926	N/A	ANDA	ANDA216521	ScieGen Pharmaceuticals, Inc	DILTIAZEM HYDROCHLORIDE	90 mg/1	500 TABLET in 1 BOTTLE (50228-483-05)
50228-483-10	50228-483	HUMAN PRESCRIPTION DRUG	Diltiazem Hydrochloride	Diltiazem Hydrochloride	TABLET	ORAL	20220926	N/A	ANDA	ANDA216521	ScieGen Pharmaceuticals, Inc	DILTIAZEM HYDROCHLORIDE	90 mg/1	1000 TABLET in 1 BOTTLE (50228-483-10)
50228-483-30	50228-483	HUMAN PRESCRIPTION DRUG	Diltiazem Hydrochloride	Diltiazem Hydrochloride	TABLET	ORAL	20220926	N/A	ANDA	ANDA216521	ScieGen Pharmaceuticals, Inc	DILTIAZEM HYDROCHLORIDE	90 mg/1	30 TABLET in 1 BOTTLE (50228-483-30)
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)