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=ANDA078401"
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
80425-0081-2 80425-0081 HUMAN PRESCRIPTION DRUG Baclofen Baclofen TABLET ORAL 20110101 N/A ANDA ANDA078401 Advanced Rx Pharmacy of Tennessee, LLC BACLOFEN 20 mg/1 60 TABLET in 1 BOTTLE (80425-0081-2)
16714-072-04 16714-072 HUMAN PRESCRIPTION DRUG Baclofen Baclofen TABLET ORAL 20110101 N/A ANDA ANDA078401 Northstar RxLLC BACLOFEN 20 mg/1 100 TABLET in 1 BOTTLE (16714-072-04)
16714-072-05 16714-072 HUMAN PRESCRIPTION DRUG Baclofen Baclofen TABLET ORAL 20110101 N/A ANDA ANDA078401 Northstar RxLLC BACLOFEN 20 mg/1 500 TABLET in 1 BOTTLE (16714-072-05)
71610-446-45 71610-446 HUMAN PRESCRIPTION DRUG Baclofen Baclofen TABLET ORAL 20200721 N/A ANDA ANDA078401 Aphena Pharma Solutions - Tennessee, LLC BACLOFEN 20 mg/1 45 TABLET in 1 BOTTLE (71610-446-45)
71610-446-60 71610-446 HUMAN PRESCRIPTION DRUG Baclofen Baclofen TABLET ORAL 20200721 N/A ANDA ANDA078401 Aphena Pharma Solutions - Tennessee, LLC BACLOFEN 20 mg/1 90 TABLET in 1 BOTTLE (71610-446-60)
71610-446-92 71610-446 HUMAN PRESCRIPTION DRUG Baclofen Baclofen TABLET ORAL 20200730 N/A ANDA ANDA078401 Aphena Pharma Solutions - Tennessee, LLC BACLOFEN 20 mg/1 270 TABLET in 1 BOTTLE (71610-446-92)
63739-480-10 63739-480 HUMAN PRESCRIPTION DRUG Baclofen Baclofen TABLET ORAL 20160504 N/A ANDA ANDA078401 Mckesson Corporation DBA SKY Packaginng BACLOFEN 20 mg/1 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-480-10) / 10 TABLET in 1 BLISTER PACK
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