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=ANDA200895"
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
31722-513-90 31722-513 HUMAN PRESCRIPTION DRUG Simvastatin Simvastatin TABLET, FILM COATED ORAL 20141203 N/A ANDA ANDA200895 Camber Pharmaceuticals, Inc. SIMVASTATIN 40 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (31722-513-90)
31722-514-05 31722-514 HUMAN PRESCRIPTION DRUG Simvastatin Simvastatin TABLET, FILM COATED ORAL 20141209 N/A ANDA ANDA200895 Camber Pharmaceuticals, Inc. SIMVASTATIN 80 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (31722-514-05)
31722-514-30 31722-514 HUMAN PRESCRIPTION DRUG Simvastatin Simvastatin TABLET, FILM COATED ORAL 20141209 N/A ANDA ANDA200895 Camber Pharmaceuticals, Inc. SIMVASTATIN 80 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (31722-514-30)
31722-514-90 31722-514 HUMAN PRESCRIPTION DRUG Simvastatin Simvastatin TABLET, FILM COATED ORAL 20141209 N/A ANDA ANDA200895 Camber Pharmaceuticals, Inc. SIMVASTATIN 80 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (31722-514-90)
31722-514-01 31722-514 HUMAN PRESCRIPTION DRUG Simvastatin Simvastatin TABLET, FILM COATED ORAL 20141209 N/A ANDA ANDA200895 Camber Pharmaceuticals, Inc. SIMVASTATIN 80 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (31722-514-01)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase