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=ANDA090818"
符合检索条件的记录共 18 条，共 1 页，当前第 1 页 ，可点击列名称排序
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
47335-724-64 47335-724 HUMAN OTC DRUG Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20180301 N/A ANDA ANDA090818 Sun Pharmaceutical Industries, Inc. FEXOFENADINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE 60 mg/1; 120 mg/1 6 BLISTER PACK in 1 CARTON (47335-724-64) / 5 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
47335-724-66 47335-724 HUMAN OTC DRUG Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20180301 N/A ANDA ANDA090818 Sun Pharmaceutical Industries, Inc. FEXOFENADINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE 60 mg/1; 120 mg/1 2 BLISTER PACK in 1 CARTON (47335-724-66) / 5 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
47335-724-75 47335-724 HUMAN OTC DRUG Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20180301 N/A ANDA ANDA090818 Sun Pharmaceutical Industries, Inc. FEXOFENADINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE 60 mg/1; 120 mg/1 4 BLISTER PACK in 1 CARTON (47335-724-75) / 5 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
47335-724-83 47335-724 HUMAN OTC DRUG Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20180301 N/A ANDA ANDA090818 Sun Pharmaceutical Industries, Inc. FEXOFENADINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE 60 mg/1; 120 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-724-83)
47335-724-94 47335-724 HUMAN OTC DRUG Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20180301 N/A ANDA ANDA090818 Sun Pharmaceutical Industries, Inc. FEXOFENADINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE 60 mg/1; 120 mg/1 1 BLISTER PACK in 1 CARTON (47335-724-94) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
47335-724-95 47335-724 HUMAN OTC DRUG Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20180301 N/A ANDA ANDA090818 Sun Pharmaceutical Industries, Inc. FEXOFENADINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE 60 mg/1; 120 mg/1 3 BLISTER PACK in 1 CARTON (47335-724-95) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
69842-990-20 69842-990 HUMAN OTC DRUG Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20180301 N/A ANDA ANDA090818 CVS Pharmacy FEXOFENADINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE 60 mg/1; 120 mg/1 1 BLISTER PACK in 1 CARTON (69842-990-20) / 20 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
69842-990-30 69842-990 HUMAN OTC DRUG Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20180301 N/A ANDA ANDA090818 CVS Pharmacy FEXOFENADINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE 60 mg/1; 120 mg/1 1 BLISTER PACK in 1 CARTON (69842-990-30) / 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
46122-452-60 46122-452 HUMAN OTC DRUG Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20180301 N/A ANDA ANDA090818 AmeriSource Bergen FEXOFENADINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE 60 mg/1; 120 mg/1 1 BLISTER PACK in 1 CARTON (46122-452-60) / 20 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
41415-995-20 41415-995 HUMAN OTC DRUG Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride fexofenadine hydrochloride and pseudoephedrine hydrochloride TABLET, EXTENDED RELEASE ORAL 20211108 N/A ANDA ANDA090818 PUBLIX SUPER MARKETS, INC FEXOFENADINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE 60 mg/1; 120 mg/1 1 BLISTER PACK in 1 CARTON (41415-995-20) / 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
41415-995-30 41415-995 HUMAN OTC DRUG Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride fexofenadine hydrochloride and pseudoephedrine hydrochloride TABLET, EXTENDED RELEASE ORAL 20211108 N/A ANDA ANDA090818 PUBLIX SUPER MARKETS, INC FEXOFENADINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE 60 mg/1; 120 mg/1 1 BLISTER PACK in 1 CARTON (41415-995-30) / 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
46122-694-65 46122-694 HUMAN OTC DRUG Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20180301 N/A ANDA ANDA090818 AmeriSource Bergen FEXOFENADINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE 60 mg/1; 120 mg/1 3 BLISTER PACK in 1 CARTON (46122-694-65) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
47335-724-99 47335-724 HUMAN OTC DRUG Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20180301 N/A ANDA ANDA090818 Sun Pharmaceutical Industries, Inc. FEXOFENADINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE 60 mg/1; 120 mg/1 2 BLISTER PACK in 1 CARTON (47335-724-99) / 10 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
51660-037-21 51660-037 HUMAN OTC DRUG Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20180301 N/A ANDA ANDA090818 Ohm Laboratories Inc. FEXOFENADINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE 60 mg/1; 120 mg/1 1 BLISTER PACK in 1 CARTON (51660-037-21) / 20 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
51660-037-31 51660-037 HUMAN OTC DRUG Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20180301 N/A ANDA ANDA090818 Ohm Laboratories Inc. FEXOFENADINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE 60 mg/1; 120 mg/1 1 BLISTER PACK in 1 CARTON (51660-037-31) / 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
37808-999-30 37808-999 HUMAN OTC DRUG Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20180801 N/A ANDA ANDA090818 H E B FEXOFENADINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE 60 mg/1; 120 mg/1 1 BLISTER PACK in 1 CARTON (37808-999-30) / 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK
69842-973-20 69842-973 HUMAN OTC DRUG Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride FEXOFENADINE HYDROCHLORIDE AND PSEUDOEPHEDRINE HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20200827 N/A ANDA ANDA090818 CVS Pharmacy FEXOFENADINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE 60 mg/1; 120 mg/1 1 BLISTER PACK in 1 CARTON (69842-973-20) / 20 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
69842-973-30 69842-973 HUMAN OTC DRUG Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride FEXOFENADINE HYDROCHLORIDE AND PSEUDOEPHEDRINE HYDROCHLORIDE TABLET, EXTENDED RELEASE ORAL 20200827 N/A ANDA ANDA090818 CVS Pharmacy FEXOFENADINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE 60 mg/1; 120 mg/1 1 BLISTER PACK in 1 CARTON (69842-973-30) / 30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
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