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
68788-8193-6 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 60 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-8193-6)
68788-8193-8 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/1 120 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-8193-8)
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)
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)
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)
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