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
47335-679-81	47335-679	HUMAN PRESCRIPTION DRUG	Diltiazem Hydrochloride	Diltiazem Hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20111031	N/A	ANDA	ANDA090492	Sun Pharmaceutical Industries, Inc.	DILTIAZEM HYDROCHLORIDE	360 mg/1	90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (47335-679-81)
47335-679-83	47335-679	HUMAN PRESCRIPTION DRUG	Diltiazem Hydrochloride	Diltiazem Hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20111031	N/A	ANDA	ANDA090492	Sun Pharmaceutical Industries, Inc.	DILTIAZEM HYDROCHLORIDE	360 mg/1	30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (47335-679-83)
47335-675-19	47335-675	HUMAN PRESCRIPTION DRUG	Diltiazem Hydrochloride	Diltiazem Hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20111031	N/A	ANDA	ANDA090492	Sun Pharmaceutical Industries, Inc.	DILTIAZEM HYDROCHLORIDE	120 mg/1	90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (47335-675-19)
47335-675-18	47335-675	HUMAN PRESCRIPTION DRUG	Diltiazem Hydrochloride	Diltiazem Hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20111031	N/A	ANDA	ANDA090492	Sun Pharmaceutical Industries, Inc.	DILTIAZEM HYDROCHLORIDE	120 mg/1	1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (47335-675-18)
47335-675-13	47335-675	HUMAN PRESCRIPTION DRUG	Diltiazem Hydrochloride	Diltiazem Hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20111031	N/A	ANDA	ANDA090492	Sun Pharmaceutical Industries, Inc.	DILTIAZEM HYDROCHLORIDE	120 mg/1	500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (47335-675-13)