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=ANDA204071"
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
63629-8849-1 63629-8849 HUMAN PRESCRIPTION DRUG SODIUM POLYSTYRENE SULFONATE sodium polystyrene sulfonate POWDER, FOR SUSPENSION ORAL; RECTAL 20210920 N/A ANDA ANDA204071 Bryant Ranch Prepack SODIUM POLYSTYRENE SULFONATE 4.1 meq/g 15 g in 1 BOTTLE (63629-8849-1)
10135-146-14 10135-146 HUMAN PRESCRIPTION DRUG Sodium Polystyrene Sulfonate sodium polystyrene sulfonate POWDER, FOR SUSPENSION ORAL; RECTAL 20160301 N/A ANDA ANDA204071 Marlex Pharmaceuticals Inc SODIUM POLYSTYRENE SULFONATE 4.1 meq/g 15 g in 1 BOTTLE, PLASTIC (10135-146-14)
10135-146-17 10135-146 HUMAN PRESCRIPTION DRUG Sodium Polystyrene Sulfonate sodium polystyrene sulfonate POWDER, FOR SUSPENSION ORAL; RECTAL 20160301 N/A ANDA ANDA204071 Marlex Pharmaceuticals Inc SODIUM POLYSTYRENE SULFONATE 4.1 meq/g 454 g in 1 JAR (10135-146-17)
72162-1230-2 72162-1230 HUMAN PRESCRIPTION DRUG SODIUM POLYSTYRENE SULFONATE sodium polystyrene sulfonate POWDER, FOR SUSPENSION ORAL; RECTAL 20230913 N/A ANDA ANDA204071 Bryant Ranch Prepack SODIUM POLYSTYRENE SULFONATE 4.1 meq/g 454 g in 1 JAR (72162-1230-2)
63629-2390-1 63629-2390 HUMAN PRESCRIPTION DRUG SODIUM POLYSTYRENE SULFONATE sodium polystyrene sulfonate POWDER, FOR SUSPENSION ORAL; RECTAL 20210222 N/A ANDA ANDA204071 Bryant Ranch Prepack SODIUM POLYSTYRENE SULFONATE 4.1 meq/g 454 g in 1 JAR (63629-2390-1)
63629-8850-1 63629-8850 HUMAN PRESCRIPTION DRUG SODIUM POLYSTYRENE SULFONATE sodium polystyrene sulfonate POWDER, FOR SUSPENSION ORAL; RECTAL 20210920 N/A ANDA ANDA204071 Bryant Ranch Prepack SODIUM POLYSTYRENE SULFONATE 4.1 meq/g 15 g in 1 BOTTLE (63629-8850-1)
11534-166-15 11534-166 HUMAN PRESCRIPTION DRUG SODIUM POLYSTYRENE SULFONATE sodium polystyrene sulfonate POWDER, FOR SUSPENSION ORAL; RECTAL 20170124 N/A ANDA ANDA204071 SUNRISE PHARMACEUTICAL, INC. SODIUM POLYSTYRENE SULFONATE 4.1 meq/g 15 g in 1 BOTTLE (11534-166-15)
11534-166-16 11534-166 HUMAN PRESCRIPTION DRUG SODIUM POLYSTYRENE SULFONATE sodium polystyrene sulfonate POWDER, FOR SUSPENSION ORAL; RECTAL 20170124 N/A ANDA ANDA204071 SUNRISE PHARMACEUTICAL, INC. SODIUM POLYSTYRENE SULFONATE 4.1 meq/g 15 g in 1 BOTTLE (11534-166-16)
11534-166-44 11534-166 HUMAN PRESCRIPTION DRUG SODIUM POLYSTYRENE SULFONATE sodium polystyrene sulfonate POWDER, FOR SUSPENSION ORAL; RECTAL 20170124 N/A ANDA ANDA204071 SUNRISE PHARMACEUTICAL, INC. SODIUM POLYSTYRENE SULFONATE 4.1 meq/g 454 g in 1 JAR (11534-166-44)
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