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=ANDA203995"
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
65162-436-03 65162-436 HUMAN PRESCRIPTION DRUG Diclofenac Sodium and Misoprostol Diclofenac Sodium and Misoprostol TABLET, DELAYED RELEASE ORAL 20161201 N/A ANDA ANDA203995 Amneal Pharmaceuticals LLC DICLOFENAC SODIUM; MISOPROSTOL 50 mg/1; 200 ug/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (65162-436-03)
65162-436-06 65162-436 HUMAN PRESCRIPTION DRUG Diclofenac Sodium and Misoprostol Diclofenac Sodium and Misoprostol TABLET, DELAYED RELEASE ORAL 20161201 N/A ANDA ANDA203995 Amneal Pharmaceuticals LLC DICLOFENAC SODIUM; MISOPROSTOL 50 mg/1; 200 ug/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE (65162-436-06)
65162-436-09 65162-436 HUMAN PRESCRIPTION DRUG Diclofenac Sodium and Misoprostol Diclofenac Sodium and Misoprostol TABLET, DELAYED RELEASE ORAL 20161201 N/A ANDA ANDA203995 Amneal Pharmaceuticals LLC DICLOFENAC SODIUM; MISOPROSTOL 50 mg/1; 200 ug/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (65162-436-09)
65162-436-10 65162-436 HUMAN PRESCRIPTION DRUG Diclofenac Sodium and Misoprostol Diclofenac Sodium and Misoprostol TABLET, DELAYED RELEASE ORAL 20161201 N/A ANDA ANDA203995 Amneal Pharmaceuticals LLC DICLOFENAC SODIUM; MISOPROSTOL 50 mg/1; 200 ug/1 100 TABLET, DELAYED RELEASE in 1 BOTTLE (65162-436-10)
65162-438-03 65162-438 HUMAN PRESCRIPTION DRUG Diclofenac Sodium and Misoprostol Diclofenac Sodium and Misoprostol TABLET, DELAYED RELEASE ORAL 20161201 N/A ANDA ANDA203995 Amneal Pharmaceuticals LLC DICLOFENAC SODIUM; MISOPROSTOL 75 mg/1; 200 ug/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (65162-438-03)
65162-438-06 65162-438 HUMAN PRESCRIPTION DRUG Diclofenac Sodium and Misoprostol Diclofenac Sodium and Misoprostol TABLET, DELAYED RELEASE ORAL 20161201 N/A ANDA ANDA203995 Amneal Pharmaceuticals LLC DICLOFENAC SODIUM; MISOPROSTOL 75 mg/1; 200 ug/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE (65162-438-06)
65162-438-10 65162-438 HUMAN PRESCRIPTION DRUG Diclofenac Sodium and Misoprostol Diclofenac Sodium and Misoprostol TABLET, DELAYED RELEASE ORAL 20161201 N/A ANDA ANDA203995 Amneal Pharmaceuticals LLC DICLOFENAC SODIUM; MISOPROSTOL 75 mg/1; 200 ug/1 100 TABLET, DELAYED RELEASE in 1 BOTTLE (65162-438-10)
71335-1183-1 71335-1183 HUMAN PRESCRIPTION DRUG Diclofenac Sodium and Misoprostol Diclofenac Sodium and Misoprostol TABLET, DELAYED RELEASE ORAL 20250129 N/A ANDA ANDA203995 Bryant Ranch Prepack DICLOFENAC SODIUM; MISOPROSTOL 75 mg/1; 200 ug/1 20 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1183-1)
71335-1183-2 71335-1183 HUMAN PRESCRIPTION DRUG Diclofenac Sodium and Misoprostol Diclofenac Sodium and Misoprostol TABLET, DELAYED RELEASE ORAL 20190410 N/A ANDA ANDA203995 Bryant Ranch Prepack DICLOFENAC SODIUM; MISOPROSTOL 75 mg/1; 200 ug/1 14 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1183-2)
71335-1183-3 71335-1183 HUMAN PRESCRIPTION DRUG Diclofenac Sodium and Misoprostol Diclofenac Sodium and Misoprostol TABLET, DELAYED RELEASE ORAL 20250129 N/A ANDA ANDA203995 Bryant Ranch Prepack DICLOFENAC SODIUM; MISOPROSTOL 75 mg/1; 200 ug/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1183-3)
71335-1183-4 71335-1183 HUMAN PRESCRIPTION DRUG Diclofenac Sodium and Misoprostol Diclofenac Sodium and Misoprostol TABLET, DELAYED RELEASE ORAL 20250129 N/A ANDA ANDA203995 Bryant Ranch Prepack DICLOFENAC SODIUM; MISOPROSTOL 75 mg/1; 200 ug/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1183-4)
71335-1183-5 71335-1183 HUMAN PRESCRIPTION DRUG Diclofenac Sodium and Misoprostol Diclofenac Sodium and Misoprostol TABLET, DELAYED RELEASE ORAL 20250129 N/A ANDA ANDA203995 Bryant Ranch Prepack DICLOFENAC SODIUM; MISOPROSTOL 75 mg/1; 200 ug/1 10 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-1183-5)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2025 Drugfuture->U.S. FDA National Drug Code DataBase