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
68682-704-30	68682-704	HUMAN PRESCRIPTION DRUG	Diltiazem Hydrochloride	Diltiazem Hydrochloride Extended-Release Tablets	TABLET, EXTENDED RELEASE	ORAL	20191001	N/A	NDA AUTHORIZED GENERIC	NDA021392	Oceanside Pharmaceuticals	DILTIAZEM HYDROCHLORIDE	120 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68682-704-30)
68682-704-90	68682-704	HUMAN PRESCRIPTION DRUG	Diltiazem Hydrochloride	Diltiazem Hydrochloride Extended-Release Tablets	TABLET, EXTENDED RELEASE	ORAL	20191001	N/A	NDA AUTHORIZED GENERIC	NDA021392	Oceanside Pharmaceuticals	DILTIAZEM HYDROCHLORIDE	120 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68682-704-90)
68682-708-30	68682-708	HUMAN PRESCRIPTION DRUG	Diltiazem Hydrochloride	Diltiazem Hydrochloride Extended-Release Tablets	TABLET, EXTENDED RELEASE	ORAL	20140206	N/A	NDA AUTHORIZED GENERIC	NDA021392	Oceanside Pharmaceuticals	DILTIAZEM HYDROCHLORIDE	360 mg/1	30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68682-708-30)
68682-708-90	68682-708	HUMAN PRESCRIPTION DRUG	Diltiazem Hydrochloride	Diltiazem Hydrochloride Extended-Release Tablets	TABLET, EXTENDED RELEASE	ORAL	20140206	N/A	NDA AUTHORIZED GENERIC	NDA021392	Oceanside Pharmaceuticals	DILTIAZEM HYDROCHLORIDE	360 mg/1	90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68682-708-90)