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=ANDA075805"
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
63629-1014-6 63629-1014 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20110525 N/A ANDA ANDA075805 Bryant Ranch Prepack FAMOTIDINE 40 mg/1 60 TABLET in 1 BOTTLE (63629-1014-6)
63629-1014-8 63629-1014 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20110525 N/A ANDA ANDA075805 Bryant Ranch Prepack FAMOTIDINE 40 mg/1 800 TABLET in 1 BOTTLE (63629-1014-8)
63629-1013-0 63629-1013 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20120410 N/A ANDA ANDA075805 Bryant Ranch Prepack FAMOTIDINE 20 mg/1 1000 TABLET in 1 BOTTLE (63629-1013-0)
63629-1013-1 63629-1013 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20120410 N/A ANDA ANDA075805 Bryant Ranch Prepack FAMOTIDINE 20 mg/1 100 TABLET in 1 BOTTLE (63629-1013-1)
63629-1013-2 63629-1013 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20120410 N/A ANDA ANDA075805 Bryant Ranch Prepack FAMOTIDINE 20 mg/1 30 TABLET in 1 BOTTLE (63629-1013-2)
43063-695-20 43063-695 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20170221 N/A ANDA ANDA075805 PD-Rx Pharmaceuticals, Inc. FAMOTIDINE 20 mg/1 20 TABLET in 1 BOTTLE, PLASTIC (43063-695-20)
43063-695-93 43063-695 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20160726 N/A ANDA ANDA075805 PD-Rx Pharmaceuticals, Inc. FAMOTIDINE 20 mg/1 180 TABLET in 1 BOTTLE, PLASTIC (43063-695-93)
43063-695-95 43063-695 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20210222 N/A ANDA ANDA075805 PD-Rx Pharmaceuticals, Inc. FAMOTIDINE 20 mg/1 1000 TABLET in 1 BOTTLE, PLASTIC (43063-695-95)
43063-696-30 43063-696 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20160726 N/A ANDA ANDA075805 PD-Rx Pharmaceuticals, Inc. FAMOTIDINE 40 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (43063-696-30)
43063-696-90 43063-696 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20160726 N/A ANDA ANDA075805 PD-Rx Pharmaceuticals, Inc. FAMOTIDINE 40 mg/1 90 TABLET in 1 BOTTLE, PLASTIC (43063-696-90)
43063-696-93 43063-696 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20160726 N/A ANDA ANDA075805 PD-Rx Pharmaceuticals, Inc. FAMOTIDINE 40 mg/1 180 TABLET in 1 BOTTLE, PLASTIC (43063-696-93)
43063-696-95 43063-696 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20210511 N/A ANDA ANDA075805 PD-Rx Pharmaceuticals, Inc. FAMOTIDINE 40 mg/1 1000 TABLET in 1 BOTTLE, PLASTIC (43063-696-95)
43063-695-30 43063-695 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20160726 N/A ANDA ANDA075805 PD-Rx Pharmaceuticals, Inc. FAMOTIDINE 20 mg/1 30 TABLET in 1 BOTTLE, PLASTIC (43063-695-30)
43063-695-60 43063-695 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20160726 N/A ANDA ANDA075805 PD-Rx Pharmaceuticals, Inc. FAMOTIDINE 20 mg/1 60 TABLET in 1 BOTTLE, PLASTIC (43063-695-60)
43063-695-90 43063-695 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20160726 N/A ANDA ANDA075805 PD-Rx Pharmaceuticals, Inc. FAMOTIDINE 20 mg/1 90 TABLET in 1 BOTTLE, PLASTIC (43063-695-90)
50090-1045-0 50090-1045 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20141128 N/A ANDA ANDA075805 A-S Medication Solutions FAMOTIDINE 20 mg/1 30 TABLET in 1 BOTTLE (50090-1045-0)
50090-1045-1 50090-1045 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20141128 N/A ANDA ANDA075805 A-S Medication Solutions FAMOTIDINE 20 mg/1 20 TABLET in 1 BOTTLE (50090-1045-1)
50090-1045-2 50090-1045 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20141128 N/A ANDA ANDA075805 A-S Medication Solutions FAMOTIDINE 20 mg/1 60 TABLET in 1 BOTTLE (50090-1045-2)
55154-6843-0 55154-6843 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20150129 N/A ANDA ANDA075805 Cardinal Health 107, LLC FAMOTIDINE 20 mg/1 10 BLISTER PACK in 1 BAG (55154-6843-0) / 1 TABLET in 1 BLISTER PACK
60760-327-07 60760-327 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET ORAL 20201218 N/A ANDA ANDA075805 St. Mary's Medical Park Pharmacy FAMOTIDINE 40 mg/1 7 TABLET in 1 BOTTLE, PLASTIC (60760-327-07)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase