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=ANDA212067"
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
80425-0391-4 80425-0391 HUMAN PRESCRIPTION DRUG Baclofen Baclofen TABLET ORAL 20240523 N/A ANDA ANDA212067 Advanced Rx Pharmacy of Tennessee, LLC BACLOFEN 10 mg/1 120 TABLET in 1 BOTTLE (80425-0391-4)
80425-0391-3 80425-0391 HUMAN PRESCRIPTION DRUG Baclofen Baclofen TABLET ORAL 20240523 N/A ANDA ANDA212067 Advanced Rx Pharmacy of Tennessee, LLC BACLOFEN 10 mg/1 90 TABLET in 1 BOTTLE (80425-0391-3)
80425-0391-2 80425-0391 HUMAN PRESCRIPTION DRUG Baclofen Baclofen TABLET ORAL 20240523 N/A ANDA ANDA212067 Advanced Rx Pharmacy of Tennessee, LLC BACLOFEN 10 mg/1 60 TABLET in 1 BOTTLE (80425-0391-2)
80425-0391-1 80425-0391 HUMAN PRESCRIPTION DRUG Baclofen Baclofen TABLET ORAL 20240523 N/A ANDA ANDA212067 Advanced Rx Pharmacy of Tennessee, LLC BACLOFEN 10 mg/1 30 TABLET in 1 BOTTLE (80425-0391-1)
80425-0459-1 80425-0459 HUMAN PRESCRIPTION DRUG Baclofen Baclofen TABLET ORAL 20241218 N/A ANDA ANDA212067 Advanced Rx of Tennessee, LLC BACLOFEN 20 mg/1 30 TABLET in 1 BOTTLE (80425-0459-1)
70518-4249-0 70518-4249 HUMAN PRESCRIPTION DRUG Baclofen Baclofen TABLET ORAL 20241230 N/A ANDA ANDA212067 REMEDYREPACK INC. BACLOFEN 10 mg/1 30 TABLET in 1 BLISTER PACK (70518-4249-0)
70518-4249-1 70518-4249 HUMAN PRESCRIPTION DRUG Baclofen Baclofen TABLET ORAL 20250801 N/A ANDA ANDA212067 REMEDYREPACK INC. BACLOFEN 10 mg/1 90 TABLET in 1 BOTTLE, PLASTIC (70518-4249-1)
70518-4249-2 70518-4249 HUMAN PRESCRIPTION DRUG Baclofen Baclofen TABLET ORAL 20250809 N/A ANDA ANDA212067 REMEDYREPACK INC. BACLOFEN 10 mg/1 30 TABLET in 1 BLISTER PACK (70518-4249-2)
71335-2392-0 71335-2392 HUMAN PRESCRIPTION DRUG Baclofen Baclofen TABLET ORAL 20240529 N/A ANDA ANDA212067 Bryant Ranch Prepack BACLOFEN 10 mg/1 112 TABLET in 1 BOTTLE (71335-2392-0)
71335-2392-1 71335-2392 HUMAN PRESCRIPTION DRUG Baclofen Baclofen TABLET ORAL 20240529 N/A ANDA ANDA212067 Bryant Ranch Prepack BACLOFEN 10 mg/1 30 TABLET in 1 BOTTLE (71335-2392-1)
71335-2392-2 71335-2392 HUMAN PRESCRIPTION DRUG Baclofen Baclofen TABLET ORAL 20240529 N/A ANDA ANDA212067 Bryant Ranch Prepack BACLOFEN 10 mg/1 120 TABLET in 1 BOTTLE (71335-2392-2)
71335-2392-3 71335-2392 HUMAN PRESCRIPTION DRUG Baclofen Baclofen TABLET ORAL 20240529 N/A ANDA ANDA212067 Bryant Ranch Prepack BACLOFEN 10 mg/1 20 TABLET in 1 BOTTLE (71335-2392-3)
71335-2392-4 71335-2392 HUMAN PRESCRIPTION DRUG Baclofen Baclofen TABLET ORAL 20240529 N/A ANDA ANDA212067 Bryant Ranch Prepack BACLOFEN 10 mg/1 60 TABLET in 1 BOTTLE (71335-2392-4)
71335-2392-5 71335-2392 HUMAN PRESCRIPTION DRUG Baclofen Baclofen TABLET ORAL 20240529 N/A ANDA ANDA212067 Bryant Ranch Prepack BACLOFEN 10 mg/1 100 TABLET in 1 BOTTLE (71335-2392-5)
71335-2392-6 71335-2392 HUMAN PRESCRIPTION DRUG Baclofen Baclofen TABLET ORAL 20240529 N/A ANDA ANDA212067 Bryant Ranch Prepack BACLOFEN 10 mg/1 56 TABLET in 1 BOTTLE (71335-2392-6)
71335-2392-7 71335-2392 HUMAN PRESCRIPTION DRUG Baclofen Baclofen TABLET ORAL 20240529 N/A ANDA ANDA212067 Bryant Ranch Prepack BACLOFEN 10 mg/1 90 TABLET in 1 BOTTLE (71335-2392-7)
71335-2392-8 71335-2392 HUMAN PRESCRIPTION DRUG Baclofen Baclofen TABLET ORAL 20240529 N/A ANDA ANDA212067 Bryant Ranch Prepack BACLOFEN 10 mg/1 140 TABLET in 1 BOTTLE (71335-2392-8)
71335-2392-9 71335-2392 HUMAN PRESCRIPTION DRUG Baclofen Baclofen TABLET ORAL 20240529 N/A ANDA ANDA212067 Bryant Ranch Prepack BACLOFEN 10 mg/1 84 TABLET in 1 BOTTLE (71335-2392-9)
80425-0459-2 80425-0459 HUMAN PRESCRIPTION DRUG Baclofen Baclofen TABLET ORAL 20241218 N/A ANDA ANDA212067 Advanced Rx of Tennessee, LLC BACLOFEN 20 mg/1 60 TABLET in 1 BOTTLE (80425-0459-2)
80425-0459-3 80425-0459 HUMAN PRESCRIPTION DRUG Baclofen Baclofen TABLET ORAL 20241218 N/A ANDA ANDA212067 Advanced Rx of Tennessee, LLC BACLOFEN 20 mg/1 90 TABLET in 1 BOTTLE (80425-0459-3)
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