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=ANDA090682"
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
53002-0061-2 53002-0061 HUMAN PRESCRIPTION DRUG Valacyclovir Hydrochloride Valacyclovir Hydrochloride TABLET, FILM COATED ORAL 20181001 N/A ANDA ANDA090682 RPK Pharmaceuticals, Inc. VALACYCLOVIR HYDROCHLORIDE 1 g/1 4 TABLET, FILM COATED in 1 BOTTLE (53002-0061-2)
53002-0061-3 53002-0061 HUMAN PRESCRIPTION DRUG Valacyclovir Hydrochloride Valacyclovir Hydrochloride TABLET, FILM COATED ORAL 20181001 N/A ANDA ANDA090682 RPK Pharmaceuticals, Inc. VALACYCLOVIR HYDROCHLORIDE 1 g/1 10 TABLET, FILM COATED in 1 BOTTLE (53002-0061-3)
53002-0061-4 53002-0061 HUMAN PRESCRIPTION DRUG Valacyclovir Hydrochloride Valacyclovir Hydrochloride TABLET, FILM COATED ORAL 20181001 N/A ANDA ANDA090682 RPK Pharmaceuticals, Inc. VALACYCLOVIR HYDROCHLORIDE 1 g/1 14 TABLET, FILM COATED in 1 BOTTLE (53002-0061-4)
53002-0061-5 53002-0061 HUMAN PRESCRIPTION DRUG Valacyclovir Hydrochloride Valacyclovir Hydrochloride TABLET, FILM COATED ORAL 20181001 N/A ANDA ANDA090682 RPK Pharmaceuticals, Inc. VALACYCLOVIR HYDROCHLORIDE 1 g/1 20 TABLET, FILM COATED in 1 BOTTLE (53002-0061-5)
53002-0061-6 53002-0061 HUMAN PRESCRIPTION DRUG Valacyclovir Hydrochloride Valacyclovir Hydrochloride TABLET, FILM COATED ORAL 20181001 N/A ANDA ANDA090682 RPK Pharmaceuticals, Inc. VALACYCLOVIR HYDROCHLORIDE 1 g/1 21 TABLET, FILM COATED in 1 BOTTLE (53002-0061-6)
67296-1551-1 67296-1551 HUMAN PRESCRIPTION DRUG Valacyclovir Hydrochloride Valacyclovir Hydrochloride TABLET, FILM COATED ORAL 20191030 N/A ANDA ANDA090682 RedPharm Drug, Inc. VALACYCLOVIR HYDROCHLORIDE 1 g/1 21 TABLET, FILM COATED in 1 BOTTLE (67296-1551-1)
67296-1551-5 67296-1551 HUMAN PRESCRIPTION DRUG Valacyclovir Hydrochloride Valacyclovir Hydrochloride TABLET, FILM COATED ORAL 20191030 N/A ANDA ANDA090682 RedPharm Drug, Inc. VALACYCLOVIR HYDROCHLORIDE 1 g/1 5 TABLET, FILM COATED in 1 BOTTLE (67296-1551-5)
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