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
70436-193-01	70436-193	HUMAN PRESCRIPTION DRUG	Diltiazem Hydrochloride	Diltiazem Hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20220905	N/A	ANDA	ANDA216304	Slate Run Pharmaceuticals, LLC	DILTIAZEM HYDROCHLORIDE	240 mg/1	100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70436-193-01)
70436-193-02	70436-193	HUMAN PRESCRIPTION DRUG	Diltiazem Hydrochloride	Diltiazem Hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20220905	N/A	ANDA	ANDA216304	Slate Run Pharmaceuticals, LLC	DILTIAZEM HYDROCHLORIDE	240 mg/1	500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70436-193-02)
70436-192-01	70436-192	HUMAN PRESCRIPTION DRUG	Diltiazem Hydrochloride	Diltiazem Hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20220905	N/A	ANDA	ANDA216304	Slate Run Pharmaceuticals, LLC	DILTIAZEM HYDROCHLORIDE	180 mg/1	100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70436-192-01)
70436-192-02	70436-192	HUMAN PRESCRIPTION DRUG	Diltiazem Hydrochloride	Diltiazem Hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20220905	N/A	ANDA	ANDA216304	Slate Run Pharmaceuticals, LLC	DILTIAZEM HYDROCHLORIDE	180 mg/1	500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70436-192-02)
70436-191-01	70436-191	HUMAN PRESCRIPTION DRUG	Diltiazem Hydrochloride	Diltiazem Hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20220905	N/A	ANDA	ANDA216304	Slate Run Pharmaceuticals, LLC	DILTIAZEM HYDROCHLORIDE	120 mg/1	100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70436-191-01)
70436-191-02	70436-191	HUMAN PRESCRIPTION DRUG	Diltiazem Hydrochloride	Diltiazem Hydrochloride	CAPSULE, EXTENDED RELEASE	ORAL	20220905	N/A	ANDA	ANDA216304	Slate Run Pharmaceuticals, LLC	DILTIAZEM HYDROCHLORIDE	120 mg/1	500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70436-191-02)