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
42799-130-02	42799-130	HUMAN PRESCRIPTION DRUG	Diltiazem Hydrochloride	Diltiazem Hydrochloride	TABLET, FILM COATED	ORAL	20181029	N/A	ANDA	ANDA211596	Edenbridge Pharmaceuticals LLC.	DILTIAZEM HYDROCHLORIDE	60 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (42799-130-02)
42799-131-01	42799-131	HUMAN PRESCRIPTION DRUG	Diltiazem Hydrochloride	Diltiazem Hydrochloride	TABLET, FILM COATED	ORAL	20181029	N/A	ANDA	ANDA211596	Edenbridge Pharmaceuticals LLC.	DILTIAZEM HYDROCHLORIDE	90 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (42799-131-01)
42799-131-02	42799-131	HUMAN PRESCRIPTION DRUG	Diltiazem Hydrochloride	Diltiazem Hydrochloride	TABLET, FILM COATED	ORAL	20181029	N/A	ANDA	ANDA211596	Edenbridge Pharmaceuticals LLC.	DILTIAZEM HYDROCHLORIDE	90 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (42799-131-02)
42799-132-01	42799-132	HUMAN PRESCRIPTION DRUG	Diltiazem Hydrochloride	Diltiazem Hydrochloride	TABLET, FILM COATED	ORAL	20181029	N/A	ANDA	ANDA211596	Edenbridge Pharmaceuticals LLC.	DILTIAZEM HYDROCHLORIDE	120 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (42799-132-01)
42799-130-01	42799-130	HUMAN PRESCRIPTION DRUG	Diltiazem Hydrochloride	Diltiazem Hydrochloride	TABLET, FILM COATED	ORAL	20181029	N/A	ANDA	ANDA211596	Edenbridge Pharmaceuticals LLC.	DILTIAZEM HYDROCHLORIDE	60 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (42799-130-01)
42799-129-02	42799-129	HUMAN PRESCRIPTION DRUG	Diltiazem Hydrochloride	Diltiazem Hydrochloride	TABLET, FILM COATED	ORAL	20181029	N/A	ANDA	ANDA211596	Edenbridge Pharmaceuticals LLC.	DILTIAZEM HYDROCHLORIDE	30 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (42799-129-02)
42799-129-01	42799-129	HUMAN PRESCRIPTION DRUG	Diltiazem Hydrochloride	Diltiazem Hydrochloride	TABLET, FILM COATED	ORAL	20181029	N/A	ANDA	ANDA211596	Edenbridge Pharmaceuticals LLC.	DILTIAZEM HYDROCHLORIDE	30 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (42799-129-01)