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=ANDA209908"
符合检索条件的记录共 13 条，共 1 页，当前第 1 页 ，可点击列名称排序
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
31722-646-30 31722-646 HUMAN PRESCRIPTION DRUG Tadalafil Tadalafil TABLET, FILM COATED ORAL 20190326 N/A ANDA ANDA209908 Camber Pharmaceuticals, Inc. TADALAFIL 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (31722-646-30)
31722-646-31 31722-646 HUMAN PRESCRIPTION DRUG Tadalafil Tadalafil TABLET, FILM COATED ORAL 20190326 N/A ANDA ANDA209908 Camber Pharmaceuticals, Inc. TADALAFIL 20 mg/1 10 BLISTER PACK in 1 CARTON (31722-646-31) / 10 TABLET, FILM COATED in 1 BLISTER PACK
50090-6945-0 50090-6945 HUMAN PRESCRIPTION DRUG Tadalafil Tadalafil TABLET, FILM COATED ORAL 20231218 N/A ANDA ANDA209908 A-S Medication Solutions TADALAFIL 5 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (50090-6945-0)
31722-644-30 31722-644 HUMAN PRESCRIPTION DRUG Tadalafil Tadalafil TABLET, FILM COATED ORAL 20190326 N/A ANDA ANDA209908 Camber Pharmaceuticals, Inc. TADALAFIL 5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (31722-644-30)
31722-644-31 31722-644 HUMAN PRESCRIPTION DRUG Tadalafil Tadalafil TABLET, FILM COATED ORAL 20190326 N/A ANDA ANDA209908 Camber Pharmaceuticals, Inc. TADALAFIL 5 mg/1 3 BLISTER PACK in 1 CARTON (31722-644-31) / 10 TABLET, FILM COATED in 1 BLISTER PACK
61919-887-10 61919-887 HUMAN PRESCRIPTION DRUG Tadalafil Tadalafil TABLET, FILM COATED ORAL 20190612 N/A ANDA ANDA209908 Direct_Rx TADALAFIL 20 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (61919-887-10)
61919-887-30 61919-887 HUMAN PRESCRIPTION DRUG Tadalafil Tadalafil TABLET, FILM COATED ORAL 20190612 N/A ANDA ANDA209908 Direct_Rx TADALAFIL 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (61919-887-30)
50090-4660-0 50090-4660 HUMAN PRESCRIPTION DRUG Tadalafil Tadalafil TABLET, FILM COATED ORAL 20191029 N/A ANDA ANDA209908 A-S Medication Solutions TADALAFIL 5 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (50090-4660-0)
50090-4660-1 50090-4660 HUMAN PRESCRIPTION DRUG Tadalafil Tadalafil TABLET, FILM COATED ORAL 20191210 N/A ANDA ANDA209908 A-S Medication Solutions TADALAFIL 5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (50090-4660-1)
31722-643-30 31722-643 HUMAN PRESCRIPTION DRUG Tadalafil Tadalafil TABLET, FILM COATED ORAL 20190326 N/A ANDA ANDA209908 Camber Pharmaceuticals, Inc. TADALAFIL 2.5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (31722-643-30)
31722-643-31 31722-643 HUMAN PRESCRIPTION DRUG Tadalafil Tadalafil TABLET, FILM COATED ORAL 20190326 N/A ANDA ANDA209908 Camber Pharmaceuticals, Inc. TADALAFIL 2.5 mg/1 3 BLISTER PACK in 1 CARTON (31722-643-31) / 10 TABLET, FILM COATED in 1 BLISTER PACK
31722-645-30 31722-645 HUMAN PRESCRIPTION DRUG Tadalafil Tadalafil TABLET, FILM COATED ORAL 20190326 N/A ANDA ANDA209908 Camber Pharmaceuticals, Inc. TADALAFIL 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (31722-645-30)
31722-645-31 31722-645 HUMAN PRESCRIPTION DRUG Tadalafil Tadalafil TABLET, FILM COATED ORAL 20190326 N/A ANDA ANDA209908 Camber Pharmaceuticals, Inc. TADALAFIL 10 mg/1 10 BLISTER PACK in 1 CARTON (31722-645-31) / 10 TABLET, FILM COATED in 1 BLISTER PACK
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