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=ANDA217563"
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
42571-416-01 42571-416 HUMAN PRESCRIPTION DRUG Metolazone Metolazone TABLET ORAL 20250301 N/A ANDA ANDA217563 Micro Labs Limited METOLAZONE 2.5 mg/1 100 TABLET in 1 CONTAINER (42571-416-01)
42571-416-10 42571-416 HUMAN PRESCRIPTION DRUG Metolazone Metolazone TABLET ORAL 20250301 N/A ANDA ANDA217563 Micro Labs Limited METOLAZONE 2.5 mg/1 1000 TABLET in 1 CONTAINER (42571-416-10)
42571-418-01 42571-418 HUMAN PRESCRIPTION DRUG Metolazone Metolazone TABLET ORAL 20250301 N/A ANDA ANDA217563 Micro Labs Limited METOLAZONE 10 mg/1 100 TABLET in 1 CONTAINER (42571-418-01)
42571-418-10 42571-418 HUMAN PRESCRIPTION DRUG Metolazone Metolazone TABLET ORAL 20250301 N/A ANDA ANDA217563 Micro Labs Limited METOLAZONE 10 mg/1 1000 TABLET in 1 CONTAINER (42571-418-10)
42571-417-01 42571-417 HUMAN PRESCRIPTION DRUG Metolazone Metolazone TABLET ORAL 20250301 N/A ANDA ANDA217563 Micro Labs Limited METOLAZONE 5 mg/1 100 TABLET in 1 CONTAINER (42571-417-01)
42571-417-10 42571-417 HUMAN PRESCRIPTION DRUG Metolazone Metolazone TABLET ORAL 20250301 N/A ANDA ANDA217563 Micro Labs Limited METOLAZONE 5 mg/1 1000 TABLET in 1 CONTAINER (42571-417-10)
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