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=ANDA076667"
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
43598-823-14 43598-823 HUMAN OTC DRUG Fexofenadine HCl and Pseudoephedrine HCI Fexofenadine HCl and Pseudoephedrine HCI TABLET, EXTENDED RELEASE ORAL 20190718 N/A ANDA ANDA076667 Dr. Reddy's Laboratories Inc. FEXOFENADINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE 60 mg/1; 120 mg/1 4 BLISTER PACK in 1 CARTON (43598-823-14) / 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
43598-823-31 43598-823 HUMAN OTC DRUG Fexofenadine HCl and Pseudoephedrine HCI Fexofenadine HCl and Pseudoephedrine HCI TABLET, EXTENDED RELEASE ORAL 20190718 N/A ANDA ANDA076667 Dr. Reddy's Laboratories Inc. FEXOFENADINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE 60 mg/1; 120 mg/1 6 BLISTER PACK in 1 CARTON (43598-823-31) / 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
43598-823-35 43598-823 HUMAN OTC DRUG Fexofenadine HCl and Pseudoephedrine HCI Fexofenadine HCl and Pseudoephedrine HCI TABLET, EXTENDED RELEASE ORAL 20191031 N/A ANDA ANDA076667 Dr. Reddy's Laboratories Inc. FEXOFENADINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE 60 mg/1; 120 mg/1 2 BLISTER PACK in 1 CARTON (43598-823-35) / 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
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