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
70436-196-06	70436-196	HUMAN PRESCRIPTION DRUG	Diltiazem Hydrochloride	Diltiazem Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20230320	N/A	ANDA	ANDA216439	Slate Run Pharmaceuticals, LLC	DILTIAZEM HYDROCHLORIDE	180 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (70436-196-06)
70436-197-04	70436-197	HUMAN PRESCRIPTION DRUG	Diltiazem Hydrochloride	Diltiazem Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20230320	N/A	ANDA	ANDA216439	Slate Run Pharmaceuticals, LLC	DILTIAZEM HYDROCHLORIDE	240 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (70436-197-04)
70436-197-06	70436-197	HUMAN PRESCRIPTION DRUG	Diltiazem Hydrochloride	Diltiazem Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20230320	N/A	ANDA	ANDA216439	Slate Run Pharmaceuticals, LLC	DILTIAZEM HYDROCHLORIDE	240 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (70436-197-06)
70436-198-04	70436-198	HUMAN PRESCRIPTION DRUG	Diltiazem Hydrochloride	Diltiazem Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20230320	N/A	ANDA	ANDA216439	Slate Run Pharmaceuticals, LLC	DILTIAZEM HYDROCHLORIDE	300 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (70436-198-04)
70436-198-06	70436-198	HUMAN PRESCRIPTION DRUG	Diltiazem Hydrochloride	Diltiazem Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20230320	N/A	ANDA	ANDA216439	Slate Run Pharmaceuticals, LLC	DILTIAZEM HYDROCHLORIDE	300 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (70436-198-06)
70436-199-04	70436-199	HUMAN PRESCRIPTION DRUG	Diltiazem Hydrochloride	Diltiazem Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20230320	N/A	ANDA	ANDA216439	Slate Run Pharmaceuticals, LLC	DILTIAZEM HYDROCHLORIDE	360 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (70436-199-04)
70436-199-06	70436-199	HUMAN PRESCRIPTION DRUG	Diltiazem Hydrochloride	Diltiazem Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20230320	N/A	ANDA	ANDA216439	Slate Run Pharmaceuticals, LLC	DILTIAZEM HYDROCHLORIDE	360 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (70436-199-06)
70436-200-04	70436-200	HUMAN PRESCRIPTION DRUG	Diltiazem Hydrochloride	Diltiazem Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20230320	N/A	ANDA	ANDA216439	Slate Run Pharmaceuticals, LLC	DILTIAZEM HYDROCHLORIDE	420 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (70436-200-04)
70436-200-06	70436-200	HUMAN PRESCRIPTION DRUG	Diltiazem Hydrochloride	Diltiazem Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20230320	N/A	ANDA	ANDA216439	Slate Run Pharmaceuticals, LLC	DILTIAZEM HYDROCHLORIDE	420 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (70436-200-06)
70436-196-04	70436-196	HUMAN PRESCRIPTION DRUG	Diltiazem Hydrochloride	Diltiazem Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20230320	N/A	ANDA	ANDA216439	Slate Run Pharmaceuticals, LLC	DILTIAZEM HYDROCHLORIDE	180 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (70436-196-04)
70436-195-06	70436-195	HUMAN PRESCRIPTION DRUG	Diltiazem Hydrochloride	Diltiazem Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20230320	N/A	ANDA	ANDA216439	Slate Run Pharmaceuticals, LLC	DILTIAZEM HYDROCHLORIDE	120 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (70436-195-06)
70436-195-04	70436-195	HUMAN PRESCRIPTION DRUG	Diltiazem Hydrochloride	Diltiazem Hydrochloride	TABLET, EXTENDED RELEASE	ORAL	20230320	N/A	ANDA	ANDA216439	Slate Run Pharmaceuticals, LLC	DILTIAZEM HYDROCHLORIDE	120 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (70436-195-04)