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=ANDA216332"
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
42385-962-18 42385-962 HUMAN PRESCRIPTION DRUG Abacavir and Lamivudine Abacavir and Lamivudine TABLET, FILM COATED ORAL 20220725 N/A ANDA ANDA216332 Laurus Labs Limited ABACAVIR SULFATE; LAMIVUDINE 600 mg/1; 300 mg/1 180 TABLET, FILM COATED in 1 BOTTLE (42385-962-18)
42385-962-30 42385-962 HUMAN PRESCRIPTION DRUG Abacavir and Lamivudine Abacavir and Lamivudine TABLET, FILM COATED ORAL 20220725 N/A ANDA ANDA216332 Laurus Labs Limited ABACAVIR SULFATE; LAMIVUDINE 600 mg/1; 300 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (42385-962-30)
42385-962-90 42385-962 HUMAN PRESCRIPTION DRUG Abacavir and Lamivudine Abacavir and Lamivudine TABLET, FILM COATED ORAL 20220725 N/A ANDA ANDA216332 Laurus Labs Limited ABACAVIR SULFATE; LAMIVUDINE 600 mg/1; 300 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (42385-962-90)
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