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=ANDA208175"
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
43598-626-30 43598-626 HUMAN PRESCRIPTION DRUG Phentermine and Topiramate Extended-Release Phentermine and Topiramate Extended-Release CAPSULE ORAL 20250601 N/A ANDA ANDA208175 Dr.Reddys Laboratories Inc PHENTERMINE HYDROCHLORIDE; TOPIRAMATE 11.25 mg/1; 69 mg/1 30 CAPSULE in 1 BOTTLE (43598-626-30)
43598-625-30 43598-625 HUMAN PRESCRIPTION DRUG Phentermine and Topiramate Extended-Release Phentermine and Topiramate Extended-Release CAPSULE ORAL 20250601 N/A ANDA ANDA208175 Dr.Reddys Laboratories Inc PHENTERMINE HYDROCHLORIDE; TOPIRAMATE 7.5 mg/1; 46 mg/1 30 CAPSULE in 1 BOTTLE (43598-625-30)
43598-624-30 43598-624 HUMAN PRESCRIPTION DRUG Phentermine and Topiramate Extended-Release Phentermine and Topiramate Extended-Release CAPSULE ORAL 20250601 N/A ANDA ANDA208175 Dr.Reddys Laboratories Inc PHENTERMINE HYDROCHLORIDE; TOPIRAMATE 3.75 mg/1; 23 mg/1 30 CAPSULE in 1 BOTTLE (43598-624-30)
43598-627-30 43598-627 HUMAN PRESCRIPTION DRUG Phentermine and Topiramate Extended-Release Phentermine and Topiramate Extended-Release CAPSULE ORAL 20250601 N/A ANDA ANDA208175 Dr.Reddys Laboratories Inc PHENTERMINE HYDROCHLORIDE; TOPIRAMATE 15 mg/1; 92 mg/1 30 CAPSULE in 1 BOTTLE (43598-627-30)
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