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=ANDA077844"
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
68084-021-21 68084-021 HUMAN PRESCRIPTION DRUG Abacavir Abacavir TABLET, FILM COATED ORAL 20130124 N/A ANDA ANDA077844 American Health Packaging ABACAVIR SULFATE 300 mg/1 30 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-021-21) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-021-11)
0904-6874-06 0904-6874 HUMAN PRESCRIPTION DRUG Abacavir Abacavir TABLET, FILM COATED ORAL 20121217 N/A ANDA ANDA077844 Major Pharmaceuticals ABACAVIR SULFATE 300 mg/1 50 BLISTER PACK in 1 CARTON (0904-6874-06) / 1 TABLET, FILM COATED in 1 BLISTER PACK
0904-6874-04 0904-6874 HUMAN PRESCRIPTION DRUG Abacavir Abacavir TABLET, FILM COATED ORAL 20121217 N/A ANDA ANDA077844 Major Pharmaceuticals ABACAVIR SULFATE 300 mg/1 30 BLISTER PACK in 1 CARTON (0904-6874-04) / 1 TABLET, FILM COATED in 1 BLISTER PACK
65862-073-60 65862-073 HUMAN PRESCRIPTION DRUG Abacavir Abacavir TABLET, FILM COATED ORAL 20121217 N/A ANDA ANDA077844 Aurobindo Pharma Limited ABACAVIR SULFATE 300 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (65862-073-60)
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