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=ANDA212663"
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
33342-440-07 33342-440 HUMAN PRESCRIPTION DRUG Abacavir and Lamivudine Abacavir and Lamivudine TABLET, FILM COATED ORAL 20241220 N/A ANDA ANDA212663 Macleods Pharmaceuticals Limited ABACAVIR SULFATE; LAMIVUDINE 600 mg/1; 300 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (33342-440-07)
33342-440-14 33342-440 HUMAN PRESCRIPTION DRUG Abacavir and Lamivudine Abacavir and Lamivudine TABLET, FILM COATED ORAL 20241220 N/A ANDA ANDA212663 Macleods Pharmaceuticals Limited ABACAVIR SULFATE; LAMIVUDINE 600 mg/1; 300 mg/1 5 BLISTER PACK in 1 CARTON (33342-440-14) / 6 TABLET, FILM COATED in 1 BLISTER PACK (33342-440-02)
33342-440-98 33342-440 HUMAN PRESCRIPTION DRUG Abacavir and Lamivudine Abacavir and Lamivudine TABLET, FILM COATED ORAL 20241220 N/A ANDA ANDA212663 Macleods Pharmaceuticals Limited ABACAVIR SULFATE; LAMIVUDINE 600 mg/1; 300 mg/1 10 BLISTER PACK in 1 CARTON (33342-440-98) / 6 TABLET, FILM COATED in 1 BLISTER PACK (33342-440-02)
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