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=ANDA070995"
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
0591-0343-01 0591-0343 HUMAN PRESCRIPTION DRUG Verapamil Hydrochloride Verapamil Hydrochloride TABLET, FILM COATED ORAL 19861001 N/A ANDA ANDA070995 Actavis Pharma, Inc. VERAPAMIL HYDROCHLORIDE 80 mg/1 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0591-0343-01)
0591-0343-05 0591-0343 HUMAN PRESCRIPTION DRUG Verapamil Hydrochloride Verapamil Hydrochloride TABLET, FILM COATED ORAL 19861001 N/A ANDA ANDA070995 Actavis Pharma, Inc. VERAPAMIL HYDROCHLORIDE 80 mg/1 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0591-0343-05)
0591-0343-10 0591-0343 HUMAN PRESCRIPTION DRUG Verapamil Hydrochloride Verapamil Hydrochloride TABLET, FILM COATED ORAL 19861001 N/A ANDA ANDA070995 Actavis Pharma, Inc. VERAPAMIL HYDROCHLORIDE 80 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0591-0343-10)
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