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
71610-902-60 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 90 TABLET, FILM COATED in 1 BOTTLE (71610-902-60)
71610-902-70 71610-902 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20250501 N/A ANDA ANDA202413 Aphena Pharma Solutions - Tennessee, LLC IBUPROFEN 600 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (71610-902-70)
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)
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)
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)
76420-846-01 76420-846 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20240908 N/A ANDA ANDA202413 Asclemed USA, Inc. IBUPROFEN 400 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (76420-846-01)
76420-846-05 76420-846 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20240908 N/A ANDA ANDA202413 Asclemed USA, Inc. IBUPROFEN 400 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (76420-846-05)
76420-846-30 76420-846 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20240908 N/A ANDA ANDA202413 Asclemed USA, Inc. IBUPROFEN 400 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (76420-846-30)
76420-846-60 76420-846 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20240908 N/A ANDA ANDA202413 Asclemed USA, Inc. IBUPROFEN 400 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (76420-846-60)
76420-846-90 76420-846 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20240908 N/A ANDA ANDA202413 Asclemed USA, Inc. IBUPROFEN 400 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (76420-846-90)
76420-847-01 76420-847 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20240908 N/A ANDA ANDA202413 Asclemed USA, Inc. IBUPROFEN 600 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (76420-847-01)
76420-847-05 76420-847 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20240908 N/A ANDA ANDA202413 Asclemed USA, Inc. IBUPROFEN 600 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (76420-847-05)
76420-847-30 76420-847 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20240908 N/A ANDA ANDA202413 Asclemed USA, Inc. IBUPROFEN 600 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (76420-847-30)
76420-847-60 76420-847 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20240908 N/A ANDA ANDA202413 Asclemed USA, Inc. IBUPROFEN 600 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (76420-847-60)
76420-847-90 76420-847 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20240908 N/A ANDA ANDA202413 Asclemed USA, Inc. IBUPROFEN 600 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (76420-847-90)
76420-848-01 76420-848 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20240908 N/A ANDA ANDA202413 Asclemed USA, Inc. IBUPROFEN 800 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (76420-848-01)
76420-848-05 76420-848 HUMAN PRESCRIPTION DRUG Ibuprofen Ibuprofen TABLET, FILM COATED ORAL 20240908 N/A ANDA ANDA202413 Asclemed USA, Inc. IBUPROFEN 800 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (76420-848-05)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2025 Drugfuture->U.S. FDA National Drug Code DataBase