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=ANDA090066"
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
68001-279-00 68001-279 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20151221 N/A ANDA ANDA090066 BluePoint Laboratories DICLOFENAC SODIUM 25 mg/1 100 TABLET, DELAYED RELEASE in 1 BOTTLE (68001-279-00)
71335-2543-1 71335-2543 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20250108 N/A ANDA ANDA090066 Bryant Ranch Prepack DICLOFENAC SODIUM 50 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2543-1)
71335-2543-2 71335-2543 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20250108 N/A ANDA ANDA090066 Bryant Ranch Prepack DICLOFENAC SODIUM 50 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2543-2)
71335-2543-3 71335-2543 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20250108 N/A ANDA ANDA090066 Bryant Ranch Prepack DICLOFENAC SODIUM 50 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2543-3)
71335-2543-4 71335-2543 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20250108 N/A ANDA ANDA090066 Bryant Ranch Prepack DICLOFENAC SODIUM 50 mg/1 120 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2543-4)
71335-2543-5 71335-2543 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20250108 N/A ANDA ANDA090066 Bryant Ranch Prepack DICLOFENAC SODIUM 50 mg/1 20 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2543-5)
71335-2543-6 71335-2543 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20250108 N/A ANDA ANDA090066 Bryant Ranch Prepack DICLOFENAC SODIUM 50 mg/1 1000 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2543-6)
71335-2543-7 71335-2543 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20250108 N/A ANDA ANDA090066 Bryant Ranch Prepack DICLOFENAC SODIUM 50 mg/1 14 TABLET, DELAYED RELEASE in 1 BOTTLE (71335-2543-7)
68001-280-00 68001-280 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20151221 N/A ANDA ANDA090066 BluePoint Laboratories DICLOFENAC SODIUM 50 mg/1 100 TABLET, DELAYED RELEASE in 1 BOTTLE (68001-280-00)
68001-280-06 68001-280 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20151221 N/A ANDA ANDA090066 BluePoint Laboratories DICLOFENAC SODIUM 50 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE (68001-280-06)
68001-280-08 68001-280 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20151221 N/A ANDA ANDA090066 BluePoint Laboratories DICLOFENAC SODIUM 50 mg/1 1000 TABLET, DELAYED RELEASE in 1 BOTTLE (68001-280-08)
50090-0540-0 50090-0540 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20141128 N/A ANDA ANDA090066 A-S Medication Solutions DICLOFENAC SODIUM 50 mg/1 100 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-0540-0)
50090-0540-2 50090-0540 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20141128 N/A ANDA ANDA090066 A-S Medication Solutions DICLOFENAC SODIUM 50 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-0540-2)
50090-0540-5 50090-0540 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20220328 N/A ANDA ANDA090066 A-S Medication Solutions DICLOFENAC SODIUM 50 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (50090-0540-5)
68788-8784-8 68788-8784 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20241212 N/A ANDA ANDA090066 Preferred Pharmaceuticals Inc. DICLOFENAC SODIUM 50 mg/1 120 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-8784-8)
68788-8784-9 68788-8784 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20241212 N/A ANDA ANDA090066 Preferred Pharmaceuticals Inc. DICLOFENAC SODIUM 50 mg/1 90 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-8784-9)
68788-8784-1 68788-8784 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20241212 N/A ANDA ANDA090066 Preferred Pharmaceuticals Inc. DICLOFENAC SODIUM 50 mg/1 100 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-8784-1)
68788-8784-3 68788-8784 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20241212 N/A ANDA ANDA090066 Preferred Pharmaceuticals Inc. DICLOFENAC SODIUM 50 mg/1 30 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-8784-3)
68788-8784-6 68788-8784 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20241212 N/A ANDA ANDA090066 Preferred Pharmaceuticals Inc. DICLOFENAC SODIUM 50 mg/1 60 TABLET, DELAYED RELEASE in 1 BOTTLE (68788-8784-6)
60687-606-01 60687-606 HUMAN PRESCRIPTION DRUG Diclofenac Sodium Diclofenac Sodium TABLET, DELAYED RELEASE ORAL 20220607 N/A ANDA ANDA090066 American Health Packaging DICLOFENAC SODIUM 50 mg/1 100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-606-01) / 1 TABLET, DELAYED RELEASE in 1 BLISTER PACK (60687-606-11)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2026 Drugfuture->U.S. FDA National Drug Code DataBase