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=ANDA209599"
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
51224-009-20 51224-009 HUMAN PRESCRIPTION DRUG Cholestyramine Light Cholestyramine POWDER, FOR SUSPENSION ORAL 20201112 N/A ANDA ANDA209599 TAGI Pharma, Inc. CHOLESTYRAMINE 4 g/4.8g 60 POUCH in 1 CARTON (51224-009-20) / 4.8 g in 1 POUCH
51224-009-10 51224-009 HUMAN PRESCRIPTION DRUG Cholestyramine Light Cholestyramine POWDER, FOR SUSPENSION ORAL 20201112 N/A ANDA ANDA209599 TAGI Pharma, Inc. CHOLESTYRAMINE 4 g/4.8g 201.6 g in 1 CAN (51224-009-10)
68094-906-20 68094-906 HUMAN PRESCRIPTION DRUG Cholestyramine Cholestyramine POWDER, FOR SUSPENSION ORAL 20231215 N/A ANDA ANDA209599 Precision Dose, Inc. CHOLESTYRAMINE 4 g/4.8g 60 POUCH in 1 CARTON (68094-906-20) / 4.8 g in 1 POUCH
68094-906-10 68094-906 HUMAN PRESCRIPTION DRUG Cholestyramine Cholestyramine POWDER, FOR SUSPENSION ORAL 20231215 N/A ANDA ANDA209599 Precision Dose, Inc. CHOLESTYRAMINE 4 g/4.8g 201.6 g in 1 CAN (68094-906-10)
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