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
68788-4039-9 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)
67046-1606-3 67046-1606 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20251013 N/A ANDA ANDA202413 Coupler LLC IBUPROFEN 800 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1606-3)
67046-1646-3 67046-1646 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20260112 N/A ANDA ANDA202413 Coupler LLC IBUPROFEN 600 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1646-3)
82804-227-30 82804-227 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20250714 N/A ANDA ANDA202413 Proficient Rx LP IBUPROFEN 800 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (82804-227-30)
70512-794-90 70512-794 HUMAN PRESCRIPTION DRUG Ibuprofen ibuprofen TABLET ORAL 20250214 N/A ANDA ANDA202413 SOLA Pharmaceuticals, LLC IBUPROFEN 300 mg/1 90 TABLET in 1 BOTTLE (70512-794-90)
73614-201-03 73614-201 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20250210 N/A ANDA ANDA202413 Brisk Pharmaceuticals IBUPROFEN 800 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (73614-201-03)
85509-2396-9 85509-2396 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20250730 N/A ANDA ANDA202413 PHOENIX RX LLC IBUPROFEN 800 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (85509-2396-9)
80425-0553-2 80425-0553 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20251015 N/A ANDA ANDA202413 Advanced Rx of Tennessee, LLC IBUPROFEN 600 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (80425-0553-2)
80425-0553-3 80425-0553 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20251015 N/A ANDA ANDA202413 Advanced Rx of Tennessee, LLC IBUPROFEN 600 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (80425-0553-3)
80425-0553-4 80425-0553 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20251015 N/A ANDA ANDA202413 Advanced Rx of Tennessee, LLC IBUPROFEN 600 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (80425-0553-4)
80425-0553-1 80425-0553 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20251015 N/A ANDA ANDA202413 Advanced Rx of Tennessee, LLC IBUPROFEN 600 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (80425-0553-1)
85509-2396-3 85509-2396 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20250730 N/A ANDA ANDA202413 PHOENIX RX LLC IBUPROFEN 800 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (85509-2396-3)
85509-2396-6 85509-2396 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20250730 N/A ANDA ANDA202413 PHOENIX RX LLC IBUPROFEN 800 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (85509-2396-6)
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)
11788-008-01 11788-008 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20251215 N/A ANDA ANDA202413 AiPing Pharmaceutical, Inc. IBUPROFEN 400 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (11788-008-01)
11788-008-05 11788-008 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20251215 N/A ANDA ANDA202413 AiPing Pharmaceutical, Inc. IBUPROFEN 400 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (11788-008-05)
71610-901-60 71610-901 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20250501 N/A ANDA ANDA202413 Aphena Pharma Solutions - Tennessee, LLC IBUPROFEN 800 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71610-901-60)
71610-901-70 71610-901 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20250501 N/A ANDA ANDA202413 Aphena Pharma Solutions - Tennessee, LLC IBUPROFEN 800 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (71610-901-70)
71610-901-80 71610-901 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20250501 N/A ANDA ANDA202413 Aphena Pharma Solutions - Tennessee, LLC IBUPROFEN 800 mg/1 180 TABLET, FILM COATED in 1 BOTTLE (71610-901-80)
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