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=ANDA078504"
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
16714-071-04 16714-071 HUMAN PRESCRIPTION DRUG Baclofen Baclofen TABLET ORAL 20110101 N/A ANDA ANDA078504 Northstar RxLLC BACLOFEN 10 mg/1 100 TABLET in 1 BOTTLE (16714-071-04)
16714-071-06 16714-071 HUMAN PRESCRIPTION DRUG Baclofen Baclofen TABLET ORAL 20110101 N/A ANDA ANDA078504 Northstar RxLLC BACLOFEN 10 mg/1 1000 TABLET in 1 BOTTLE (16714-071-06)
71205-474-14 71205-474 HUMAN PRESCRIPTION DRUG Baclofen Baclofen TABLET ORAL 20220105 N/A ANDA ANDA078504 Proficient Rx LP BACLOFEN 10 mg/1 14 TABLET in 1 BOTTLE (71205-474-14)
71205-474-20 71205-474 HUMAN PRESCRIPTION DRUG Baclofen Baclofen TABLET ORAL 20201001 N/A ANDA ANDA078504 Proficient Rx LP BACLOFEN 10 mg/1 20 TABLET in 1 BOTTLE (71205-474-20)
71205-474-30 71205-474 HUMAN PRESCRIPTION DRUG Baclofen Baclofen TABLET ORAL 20200827 N/A ANDA ANDA078504 Proficient Rx LP BACLOFEN 10 mg/1 30 TABLET in 1 BOTTLE (71205-474-30)
71205-474-60 71205-474 HUMAN PRESCRIPTION DRUG Baclofen Baclofen TABLET ORAL 20200827 N/A ANDA ANDA078504 Proficient Rx LP BACLOFEN 10 mg/1 60 TABLET in 1 BOTTLE (71205-474-60)
71205-474-72 71205-474 HUMAN PRESCRIPTION DRUG Baclofen Baclofen TABLET ORAL 20201222 N/A ANDA ANDA078504 Proficient Rx LP BACLOFEN 10 mg/1 120 TABLET in 1 BOTTLE (71205-474-72)
71205-474-78 71205-474 HUMAN PRESCRIPTION DRUG Baclofen Baclofen TABLET ORAL 20200925 N/A ANDA ANDA078504 Proficient Rx LP BACLOFEN 10 mg/1 180 TABLET in 1 BOTTLE (71205-474-78)
71205-474-90 71205-474 HUMAN PRESCRIPTION DRUG Baclofen Baclofen TABLET ORAL 20200827 N/A ANDA ANDA078504 Proficient Rx LP BACLOFEN 10 mg/1 90 TABLET in 1 BOTTLE (71205-474-90)
63739-479-10 63739-479 HUMAN PRESCRIPTION DRUG Baclofen Baclofen TABLET ORAL 20160504 N/A ANDA ANDA078504 Mckesson Corporation DBA SKY Packaginng BACLOFEN 10 mg/1 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-479-10) / 10 TABLET in 1 BLISTER PACK
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