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=ANDA075185"
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
71335-0481-3 71335-0481 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Delayed Release Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20180228 N/A ANDA ANDA075185 Bryant Ranch Prepack DICLOFENAC SODIUM 50 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0481-3)
71335-0481-4 71335-0481 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Delayed Release Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20180607 N/A ANDA ANDA075185 Bryant Ranch Prepack DICLOFENAC SODIUM 50 mg/1 120 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0481-4)
71335-0481-5 71335-0481 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Delayed Release Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20220405 N/A ANDA ANDA075185 Bryant Ranch Prepack DICLOFENAC SODIUM 50 mg/1 20 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0481-5)
71335-0481-6 71335-0481 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Delayed Release Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20180521 N/A ANDA ANDA075185 Bryant Ranch Prepack DICLOFENAC SODIUM 50 mg/1 1000 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0481-6)
71335-0481-7 71335-0481 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Delayed Release Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20190416 N/A ANDA ANDA075185 Bryant Ranch Prepack DICLOFENAC SODIUM 50 mg/1 14 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-0481-7)
68071-3184-1 68071-3184 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Delayed Release Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20170321 N/A ANDA ANDA075185 NuCare Pharmaceuticals, Inc. DICLOFENAC SODIUM 50 mg/1 21 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-3184-1)
71205-995-00 71205-995 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Delayed Release Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20200401 N/A ANDA ANDA075185 Proficient Rx LP DICLOFENAC SODIUM 50 mg/1 100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (71205-995-00)
71205-995-11 71205-995 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Delayed Release Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20200401 N/A ANDA ANDA075185 Proficient Rx LP DICLOFENAC SODIUM 50 mg/1 1000 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (71205-995-11)
71205-995-30 71205-995 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Delayed Release Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20200401 N/A ANDA ANDA075185 Proficient Rx LP DICLOFENAC SODIUM 50 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (71205-995-30)
71205-995-60 71205-995 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Delayed Release Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20200401 N/A ANDA ANDA075185 Proficient Rx LP DICLOFENAC SODIUM 50 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (71205-995-60)
71205-995-72 71205-995 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Delayed Release Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20200401 N/A ANDA ANDA075185 Proficient Rx LP DICLOFENAC SODIUM 50 mg/1 120 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (71205-995-72)
71205-995-78 71205-995 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Delayed Release Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20200401 N/A ANDA ANDA075185 Proficient Rx LP DICLOFENAC SODIUM 50 mg/1 180 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (71205-995-78)
71205-995-90 71205-995 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Delayed Release Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20200401 N/A ANDA ANDA075185 Proficient Rx LP DICLOFENAC SODIUM 50 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (71205-995-90)
68071-3184-2 68071-3184 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Delayed Release Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20170321 N/A ANDA ANDA075185 NuCare Pharmaceuticals, Inc. DICLOFENAC SODIUM 50 mg/1 20 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-3184-2)
68071-3184-3 68071-3184 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Delayed Release Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20170321 N/A ANDA ANDA075185 NuCare Pharmaceuticals, Inc. DICLOFENAC SODIUM 50 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-3184-3)
68071-3184-5 68071-3184 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Delayed Release Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20170321 N/A ANDA ANDA075185 NuCare Pharmaceuticals, Inc. DICLOFENAC SODIUM 50 mg/1 45 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-3184-5)
68071-3184-6 68071-3184 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Delayed Release Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20170321 N/A ANDA ANDA075185 NuCare Pharmaceuticals, Inc. DICLOFENAC SODIUM 50 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-3184-6)
68071-3184-9 68071-3184 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Delayed Release Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20170321 N/A ANDA ANDA075185 NuCare Pharmaceuticals, Inc. DICLOFENAC SODIUM 50 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (68071-3184-9)
51407-538-01 51407-538 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Delayed Release Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20250408 N/A ANDA ANDA075185 Golden State Medical Supply, Inc. DICLOFENAC SODIUM 75 mg/1 100 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (51407-538-01)
51407-538-10 51407-538 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Delayed Release Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20250408 N/A ANDA ANDA075185 Golden State Medical Supply, Inc. DICLOFENAC SODIUM 75 mg/1 1000 TABLET, DELAYED RELEASE in 1 BOTTLE, PLASTIC (51407-538-10)
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