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
50228-500-05	50228-500	HUMAN PRESCRIPTION DRUG	DILTIAZEM HYDROCHLORIDE	diltiazem hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20230406	N/A	ANDA	ANDA216327	ScieGen Pharmaceuticals, Inc.	DILTIAZEM HYDROCHLORIDE	420 mg/1	500 TABLET, EXTENDED RELEASE in 1 BOTTLE (50228-500-05)
50228-500-30	50228-500	HUMAN PRESCRIPTION DRUG	DILTIAZEM HYDROCHLORIDE	diltiazem hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20230406	N/A	ANDA	ANDA216327	ScieGen Pharmaceuticals, Inc.	DILTIAZEM HYDROCHLORIDE	420 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (50228-500-30)
69097-995-02	69097-995	HUMAN PRESCRIPTION DRUG	DILTIAZEM HYDROCHLORIDE	diltiazem hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20230612	N/A	ANDA	ANDA216327	Cipla USA, Inc.	DILTIAZEM HYDROCHLORIDE	300 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (69097-995-02)
69097-995-05	69097-995	HUMAN PRESCRIPTION DRUG	DILTIAZEM HYDROCHLORIDE	diltiazem hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20230612	N/A	ANDA	ANDA216327	Cipla USA, Inc.	DILTIAZEM HYDROCHLORIDE	300 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (69097-995-05)