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
68788-8193-9 68788-8193 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20220516 N/A ANDA ANDA077863 Preferred Pharmaceuticals Inc. DICLOFENAC SODIUM 75 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-8193-9)
85509-1201-3 85509-1201 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20260107 N/A ANDA ANDA077863 PHOENIX RX LLC DICLOFENAC SODIUM 75 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (85509-1201-3)
85509-1201-6 85509-1201 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20260107 N/A ANDA ANDA077863 PHOENIX RX LLC DICLOFENAC SODIUM 75 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (85509-1201-6)
85509-1201-9 85509-1201 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20260107 N/A ANDA ANDA077863 PHOENIX RX LLC DICLOFENAC SODIUM 75 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (85509-1201-9)
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)
67296-0990-2 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 20 TABLET, DELAYED RELEASE in 1 BOTTLE (67296-0990-2)
67296-0990-3 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 30 TABLET, DELAYED RELEASE in 1 BOTTLE (67296-0990-3)
67296-0990-7 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 28 TABLET, DELAYED RELEASE in 1 BOTTLE (67296-0990-7)
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)
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)
60760-090-90 60760-090 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20250625 N/A ANDA ANDA077863 St. Mary's Medical Park Pharmacy DICLOFENAC SODIUM 75 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-090-90)
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)
60760-090-30 60760-090 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20250513 N/A ANDA ANDA077863 St. Mary's Medical Park Pharmacy DICLOFENAC SODIUM 75 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (60760-090-30)
85766-010-01 85766-010 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20250618 N/A ANDA ANDA077863 Sportpharm LLC DICLOFENAC SODIUM 75 mg/1 100 TABLET, DELAYED RELEASE in 1 BOTTLE (85766-010-01)
85766-010-90 85766-010 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20250618 N/A ANDA ANDA077863 Sportpharm LLC DICLOFENAC SODIUM 75 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (85766-010-90)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2026 Drugfuture->U.S. FDA National Drug Code DataBase