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
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)
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)
50090-7788-0 50090-7788 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20251124 N/A ANDA ANDA202413 A-S Medication Solutions IBUPROFEN 400 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (50090-7788-0)
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)
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)
70518-2902-1 70518-2902 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20260423 N/A ANDA ANDA202413 REMEDYREPACK INC. IBUPROFEN 600 mg/1 50 POUCH in 1 BOX (70518-2902-1) / 1 TABLET, FILM COATED in 1 POUCH (70518-2902-2)
71610-916-60 71610-916 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20250624 N/A ANDA ANDA202413 Aphena Pharma Solutions - Tennessee, LLC IBUPROFEN 400 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71610-916-60)
71610-916-80 71610-916 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20250624 N/A ANDA ANDA202413 Aphena Pharma Solutions - Tennessee, LLC IBUPROFEN 400 mg/1 180 TABLET, FILM COATED in 1 BOTTLE (71610-916-80)
71610-916-92 71610-916 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20250624 N/A ANDA ANDA202413 Aphena Pharma Solutions - Tennessee, LLC IBUPROFEN 400 mg/1 270 TABLET, FILM COATED in 1 BOTTLE (71610-916-92)
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)
50090-7282-0 50090-7282 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 (50090-7282-0)
67296-2196-1 67296-2196 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20240523 N/A ANDA ANDA202413 Redpharm Drug IBUPROFEN 800 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (67296-2196-1)
67296-2196-3 67296-2196 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20240523 N/A ANDA ANDA202413 Redpharm Drug IBUPROFEN 800 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (67296-2196-3)
72789-565-15 72789-565 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20260605 N/A ANDA ANDA202413 PD-Rx Pharmaceuticals, Inc. IBUPROFEN 800 mg/1 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-565-15)
71610-902-80 71610-902 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20250501 N/A ANDA ANDA202413 Aphena Pharma Solutions - Tennessee, LLC IBUPROFEN 600 mg/1 180 TABLET, FILM COATED in 1 BOTTLE (71610-902-80)
71610-902-92 71610-902 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20250501 N/A ANDA ANDA202413 Aphena Pharma Solutions - Tennessee, LLC IBUPROFEN 600 mg/1 270 TABLET, FILM COATED in 1 BOTTLE (71610-902-92)
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)
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