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=ANDA202413"
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
68788-4039-1 68788-4039 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20251013 N/A ANDA ANDA202413 Preferred Pharmaceuticals Inc. IBUPROFEN 400 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (68788-4039-1)
68788-4039-2 68788-4039 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20251013 N/A ANDA ANDA202413 Preferred Pharmaceuticals Inc. IBUPROFEN 400 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (68788-4039-2)
68788-4039-3 68788-4039 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20251013 N/A ANDA ANDA202413 Preferred Pharmaceuticals Inc. IBUPROFEN 400 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68788-4039-3)
68788-4039-5 68788-4039 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20251013 N/A ANDA ANDA202413 Preferred Pharmaceuticals Inc. IBUPROFEN 400 mg/1 50 TABLET, FILM COATED in 1 BOTTLE (68788-4039-5)
68788-4039-6 68788-4039 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20251013 N/A ANDA ANDA202413 Preferred Pharmaceuticals Inc. IBUPROFEN 400 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (68788-4039-6)
68788-4039-8 68788-4039 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20251013 N/A ANDA ANDA202413 Preferred Pharmaceuticals Inc. IBUPROFEN 400 mg/1 28 TABLET, FILM COATED in 1 BOTTLE (68788-4039-8)
68788-4039-9 68788-4039 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20251013 N/A ANDA ANDA202413 Preferred Pharmaceuticals Inc. IBUPROFEN 400 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68788-4039-9)
50090-7281-5 50090-7281 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20241008 N/A ANDA ANDA202413 A-S Medication Solutions IBUPROFEN 800 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (50090-7281-5)
50090-7281-7 50090-7281 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20241008 N/A ANDA ANDA202413 A-S Medication Solutions IBUPROFEN 800 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (50090-7281-7)
11788-009-01 11788-009 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20251215 N/A ANDA ANDA202413 AiPing Pharmaceutical, Inc. IBUPROFEN 600 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (11788-009-01)
11788-009-05 11788-009 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20251215 N/A ANDA ANDA202413 AiPing Pharmaceutical, Inc. IBUPROFEN 600 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (11788-009-05)
50090-7283-0 50090-7283 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20241008 N/A ANDA ANDA202413 A-S Medication Solutions IBUPROFEN 800 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (50090-7283-0)
50090-7283-1 50090-7283 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20241008 N/A ANDA ANDA202413 A-S Medication Solutions IBUPROFEN 800 mg/1 15 TABLET, FILM COATED in 1 BOTTLE (50090-7283-1)
50090-7283-2 50090-7283 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20241008 N/A ANDA ANDA202413 A-S Medication Solutions IBUPROFEN 800 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (50090-7283-2)
50090-7283-3 50090-7283 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20241008 N/A ANDA ANDA202413 A-S Medication Solutions IBUPROFEN 800 mg/1 45 TABLET, FILM COATED in 1 BOTTLE (50090-7283-3)
50090-7283-4 50090-7283 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20241008 N/A ANDA ANDA202413 A-S Medication Solutions IBUPROFEN 800 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (50090-7283-4)
50090-7283-5 50090-7283 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20241008 N/A ANDA ANDA202413 A-S Medication Solutions IBUPROFEN 800 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (50090-7283-5)
50090-7283-7 50090-7283 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20241008 N/A ANDA ANDA202413 A-S Medication Solutions IBUPROFEN 800 mg/1 21 TABLET, FILM COATED in 1 BOTTLE (50090-7283-7)
11788-010-01 11788-010 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20251215 N/A ANDA ANDA202413 AiPing Pharmaceutical, Inc. IBUPROFEN 800 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (11788-010-01)
11788-010-05 11788-010 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20251215 N/A ANDA ANDA202413 AiPing Pharmaceutical, Inc. IBUPROFEN 800 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (11788-010-05)
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