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=ANDA077863"
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
71335-0456-0 71335-0456 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20090824 N/A ANDA ANDA077863 Bryant Ranch Prepack DICLOFENAC SODIUM 75 mg/1 40 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0456-0)
71335-0456-1 71335-0456 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20090824 N/A ANDA ANDA077863 Bryant Ranch Prepack DICLOFENAC SODIUM 75 mg/1 28 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0456-1)
71335-0456-2 71335-0456 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20090824 N/A ANDA ANDA077863 Bryant Ranch Prepack DICLOFENAC SODIUM 75 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0456-2)
71335-0456-3 71335-0456 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20090824 N/A ANDA ANDA077863 Bryant Ranch Prepack DICLOFENAC SODIUM 75 mg/1 20 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0456-3)
71335-0456-4 71335-0456 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20090824 N/A ANDA ANDA077863 Bryant Ranch Prepack DICLOFENAC SODIUM 75 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0456-4)
71335-0456-5 71335-0456 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20090824 N/A ANDA ANDA077863 Bryant Ranch Prepack DICLOFENAC SODIUM 75 mg/1 120 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0456-5)
71335-0456-6 71335-0456 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20090824 N/A ANDA ANDA077863 Bryant Ranch Prepack DICLOFENAC SODIUM 75 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0456-6)
71335-0456-7 71335-0456 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20090824 N/A ANDA ANDA077863 Bryant Ranch Prepack DICLOFENAC SODIUM 75 mg/1 100 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0456-7)
60760-090-15 60760-090 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20220705 N/A ANDA ANDA077863 St. Mary's Medical Park Pharmacy DICLOFENAC SODIUM 75 mg/1 15 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-090-15)
60760-090-20 60760-090 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20220603 N/A ANDA ANDA077863 St. Mary's Medical Park Pharmacy DICLOFENAC SODIUM 75 mg/1 20 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-090-20)
60760-090-60 60760-090 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20220707 N/A ANDA ANDA077863 St. Mary's Medical Park Pharmacy DICLOFENAC SODIUM 75 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-090-60)
16571-201-06 16571-201 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20080819 N/A ANDA ANDA077863 Rising Pharma Holdings, Inc. DICLOFENAC SODIUM 75 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (16571-201-06)
16571-201-10 16571-201 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20080819 N/A ANDA ANDA077863 Rising Pharma Holdings, Inc. DICLOFENAC SODIUM 75 mg/1 100 TABLET, DELAYED RELEASE in 1 BOTTLE (16571-201-10)
16571-201-11 16571-201 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20080819 N/A ANDA ANDA077863 Rising Pharma Holdings, Inc. DICLOFENAC SODIUM 75 mg/1 1000 TABLET, DELAYED RELEASE in 1 BOTTLE (16571-201-11)
16571-201-50 16571-201 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20080819 N/A ANDA ANDA077863 Rising Pharma Holdings, Inc. DICLOFENAC SODIUM 75 mg/1 500 TABLET, DELAYED RELEASE in 1 BOTTLE (16571-201-50)
67296-0990-1 67296-0990 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20080819 N/A ANDA ANDA077863 RedPharm Drug DICLOFENAC SODIUM 75 mg/1 21 TABLET, DELAYED RELEASE in 1 BOTTLE (67296-0990-1)
35356-714-30 35356-714 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20130207 20250831 ANDA ANDA077863 Quality Care Products LLC DICLOFENAC SODIUM 75 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (35356-714-30)
35356-714-60 35356-714 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20130207 20260731 ANDA ANDA077863 Quality Care Products LLC DICLOFENAC SODIUM 75 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE (35356-714-60)
35356-714-90 35356-714 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20130207 20250831 ANDA ANDA077863 Quality Care Products LLC DICLOFENAC SODIUM 75 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (35356-714-90)
60687-658-01 60687-658 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20220822 N/A ANDA ANDA077863 American Health Packaging DICLOFENAC SODIUM 75 mg/1 100 BLISTER PACK in 1 CARTON (60687-658-01) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (60687-658-11)
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