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=ANDA210715"
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
69097-387-19 69097-387 HUMAN PRESCRIPTION DRUG Ambrisentan Ambrisentan TABLET, FILM COATED ORAL 20190426 N/A ANDA ANDA210715 Cipla USA Inc. AMBRISENTAN 10 mg/1 1 BLISTER PACK in 1 CARTON (69097-387-19) / 10 TABLET, FILM COATED in 1 BLISTER PACK
69097-387-02 69097-387 HUMAN PRESCRIPTION DRUG Ambrisentan Ambrisentan TABLET, FILM COATED ORAL 20190426 N/A ANDA ANDA210715 Cipla USA Inc. AMBRISENTAN 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69097-387-02)
69097-386-19 69097-386 HUMAN PRESCRIPTION DRUG Ambrisentan Ambrisentan TABLET, FILM COATED ORAL 20190426 N/A ANDA ANDA210715 Cipla USA Inc. AMBRISENTAN 5 mg/1 1 BLISTER PACK in 1 CARTON (69097-386-19) / 10 TABLET, FILM COATED in 1 BLISTER PACK
69097-386-02 69097-386 HUMAN PRESCRIPTION DRUG Ambrisentan Ambrisentan TABLET, FILM COATED ORAL 20190426 N/A ANDA ANDA210715 Cipla USA Inc. AMBRISENTAN 5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69097-386-02)
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