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=ANDA210784"
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
47335-236-64 47335-236 HUMAN PRESCRIPTION DRUG ambrisentan ambrisentan TABLET, FILM COATED ORAL 20190429 N/A ANDA ANDA210784 Sun Pharmaceutical Industries, Inc. AMBRISENTAN 5 mg/1 3 BLISTER PACK in 1 CARTON (47335-236-64) / 10 TABLET, FILM COATED in 1 BLISTER PACK (47335-236-60)
47335-236-66 47335-236 HUMAN PRESCRIPTION DRUG ambrisentan ambrisentan TABLET, FILM COATED ORAL 20190429 N/A ANDA ANDA210784 Sun Pharmaceutical Industries, Inc. AMBRISENTAN 5 mg/1 1 BLISTER PACK in 1 CARTON (47335-236-66) / 10 TABLET, FILM COATED in 1 BLISTER PACK (47335-236-60)
47335-236-83 47335-236 HUMAN PRESCRIPTION DRUG ambrisentan ambrisentan TABLET, FILM COATED ORAL 20190429 N/A ANDA ANDA210784 Sun Pharmaceutical Industries, Inc. AMBRISENTAN 5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (47335-236-83)
47335-236-85 47335-236 HUMAN PRESCRIPTION DRUG ambrisentan ambrisentan TABLET, FILM COATED ORAL 20190429 N/A ANDA ANDA210784 Sun Pharmaceutical Industries, Inc. AMBRISENTAN 5 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (47335-236-85)
47335-237-64 47335-237 HUMAN PRESCRIPTION DRUG ambrisentan ambrisentan TABLET, FILM COATED ORAL 20190429 N/A ANDA ANDA210784 Sun Pharmaceutical Industries, Inc. AMBRISENTAN 10 mg/1 3 BLISTER PACK in 1 CARTON (47335-237-64) / 10 TABLET, FILM COATED in 1 BLISTER PACK (47335-237-60)
47335-237-66 47335-237 HUMAN PRESCRIPTION DRUG ambrisentan ambrisentan TABLET, FILM COATED ORAL 20190429 N/A ANDA ANDA210784 Sun Pharmaceutical Industries, Inc. AMBRISENTAN 10 mg/1 1 BLISTER PACK in 1 CARTON (47335-237-66) / 10 TABLET, FILM COATED in 1 BLISTER PACK (47335-237-60)
47335-237-83 47335-237 HUMAN PRESCRIPTION DRUG ambrisentan ambrisentan TABLET, FILM COATED ORAL 20190429 N/A ANDA ANDA210784 Sun Pharmaceutical Industries, Inc. AMBRISENTAN 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (47335-237-83)
47335-237-85 47335-237 HUMAN PRESCRIPTION DRUG ambrisentan ambrisentan TABLET, FILM COATED ORAL 20190429 N/A ANDA ANDA210784 Sun Pharmaceutical Industries, Inc. AMBRISENTAN 10 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (47335-237-85)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase