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
66267-071-14 66267-071 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20180116 N/A ANDA ANDA077863 NuCare Pharmaceuticals,Inc. DICLOFENAC SODIUM 75 mg/1 14 TABLET, DELAYED RELEASE in 1 BOTTLE (66267-071-14)
66267-071-20 66267-071 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20180116 N/A ANDA ANDA077863 NuCare Pharmaceuticals,Inc. DICLOFENAC SODIUM 75 mg/1 20 TABLET, DELAYED RELEASE in 1 BOTTLE (66267-071-20)
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)
80425-0056-1 80425-0056 HUMAN PRESCRIPTION DRUG Diclofenac DR Diclofenac TABLET, DELAYED RELEASE ORAL 20080819 N/A ANDA ANDA077863 Advanced Rx Pharmacy of Tennessee, LLC DICLOFENAC SODIUM 75 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE (80425-0056-1)
68001-281-00 68001-281 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20151221 N/A ANDA ANDA077863 BluePoint Laboratories DICLOFENAC SODIUM 75 mg/1 100 TABLET, DELAYED RELEASE in 1 BOTTLE (68001-281-00)
68001-281-03 68001-281 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20151221 N/A ANDA ANDA077863 BluePoint Laboratories DICLOFENAC SODIUM 75 mg/1 500 TABLET, DELAYED RELEASE in 1 BOTTLE (68001-281-03)
68001-281-06 68001-281 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20151221 N/A ANDA ANDA077863 BluePoint Laboratories DICLOFENAC SODIUM 75 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (68001-281-06)
68001-281-08 68001-281 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20151221 N/A ANDA ANDA077863 BluePoint Laboratories DICLOFENAC SODIUM 75 mg/1 1000 TABLET, DELAYED RELEASE in 1 BOTTLE (68001-281-08)
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)
76420-670-01 76420-670 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20240307 N/A ANDA ANDA077863 Asclemed USA, Inc. DICLOFENAC SODIUM 75 mg/1 100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (76420-670-01)
76420-670-30 76420-670 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20240307 N/A ANDA ANDA077863 Asclemed USA, Inc. DICLOFENAC SODIUM 75 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (76420-670-30)
76420-670-60 76420-670 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20240307 N/A ANDA ANDA077863 Asclemed USA, Inc. DICLOFENAC SODIUM 75 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (76420-670-60)
76420-670-90 76420-670 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20240307 N/A ANDA ANDA077863 Asclemed USA, Inc. DICLOFENAC SODIUM 75 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (76420-670-90)
67296-1480-7 67296-1480 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20151221 N/A ANDA ANDA077863 RedPharm Drug, Inc. DICLOFENAC SODIUM 75 mg/1 28 TABLET, DELAYED RELEASE in 1 BOTTLE (67296-1480-7)
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)
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