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
0187-2615-90	0187-2615	HUMAN PRESCRIPTION DRUG	TIAZAC EXTENDED RELEASE	diltiazem hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20140820	N/A	NDA	NDA020401	Bausch Health US, LLC	DILTIAZEM HYDROCHLORIDE	300 mg/1	90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0187-2615-90)
67046-1417-3	67046-1417	HUMAN PRESCRIPTION DRUG	Diltiazem Hydrochloride EXTENDED RELEASE	diltiazem hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20241111	N/A	NDA AUTHORIZED GENERIC	NDA020401	Coupler LLC	DILTIAZEM HYDROCHLORIDE	120 mg/1	30 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (67046-1417-3)
71335-0839-1	71335-0839	HUMAN PRESCRIPTION DRUG	Diltiazem Hydrochloride EXTENDED RELEASE	diltiazem hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20220128	N/A	NDA AUTHORIZED GENERIC	NDA020401	Bryant Ranch Prepack	DILTIAZEM HYDROCHLORIDE	180 mg/1	30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-0839-1)
71335-0839-2	71335-0839	HUMAN PRESCRIPTION DRUG	Diltiazem Hydrochloride EXTENDED RELEASE	diltiazem hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20180523	N/A	NDA AUTHORIZED GENERIC	NDA020401	Bryant Ranch Prepack	DILTIAZEM HYDROCHLORIDE	180 mg/1	90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-0839-2)
72189-248-90	72189-248	HUMAN PRESCRIPTION DRUG	DILTIAZEM HYDROCHLORIDE EXTENDED RELEASE	DILTIAZEM HYDROCHLORIDE EXTENDED RELEASE	CAPSULE, EXTENDED RELEASE	ORAL	20210723	N/A	NDA AUTHORIZED GENERIC	NDA020401	direct rx	DILTIAZEM HYDROCHLORIDE	240 mg/1	90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (72189-248-90)