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
0187-2617-90 0187-2617 HUMAN PRESCRIPTION DRUG TIAZAC EXTENDED RELEASE diltiazem hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20140820 N/A NDA NDA020401 Bausch Health US, LLC DILTIAZEM HYDROCHLORIDE 420 mg/1 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0187-2617-90)
0187-2613-90 0187-2613 HUMAN PRESCRIPTION DRUG TIAZAC EXTENDED RELEASE diltiazem hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20140820 N/A NDA NDA020401 Bausch Health US, LLC DILTIAZEM HYDROCHLORIDE 180 mg/1 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0187-2613-90)
0187-2612-30 0187-2612 HUMAN PRESCRIPTION DRUG TIAZAC EXTENDED RELEASE diltiazem hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20140820 N/A NDA NDA020401 Bausch Health US, LLC DILTIAZEM HYDROCHLORIDE 120 mg/1 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0187-2612-30)
0187-2612-90 0187-2612 HUMAN PRESCRIPTION DRUG TIAZAC EXTENDED RELEASE diltiazem hydrochloride CAPSULE, EXTENDED RELEASE ORAL 20140820 N/A NDA NDA020401 Bausch Health US, LLC DILTIAZEM HYDROCHLORIDE 120 mg/1 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0187-2612-90)
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