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)
检索条件:" 注册申请号=NDA020401"
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
0187-2615-90 0187-2615 HUMAN PRESCRIPTION DRUG TIAZAC EXTENDED RELEASE diltiazem hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20140820 N/A NDA NDA020401 Bausch Health US, LLC DILTIAZEM HYDROCHLORIDE 300 mg/1 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0187-2615-90)
0187-2616-30 0187-2616 HUMAN PRESCRIPTION DRUG TIAZAC EXTENDED RELEASE diltiazem hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20140820 N/A NDA NDA020401 Bausch Health US, LLC DILTIAZEM HYDROCHLORIDE 360 mg/1 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0187-2616-30)
0187-2616-90 0187-2616 HUMAN PRESCRIPTION DRUG TIAZAC EXTENDED RELEASE diltiazem hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20140820 N/A NDA NDA020401 Bausch Health US, LLC DILTIAZEM HYDROCHLORIDE 360 mg/1 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0187-2616-90)
68682-369-90 68682-369 HUMAN PRESCRIPTION DRUG Diltiazem Hydrochloride EXTENDED RELEASE diltiazem hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20140820 N/A NDA AUTHORIZED GENERIC NDA020401 Oceanside Pharmaceuticals DILTIAZEM HYDROCHLORIDE 240 mg/1 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68682-369-90)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2026 Drugfuture->U.S. FDA National Drug Code DataBase