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=ANDA079051"
符合检索条件的记录共 3 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
0378-2222-01 0378-2222 HUMAN PRESCRIPTION DRUG Nisoldipine Nisoldipine TABLET, FILM COATED, EXTENDED RELEASE ORAL 20080725 20300101 ANDA ANDA079051 Mylan Pharmaceuticals Inc. NISOLDIPINE 20 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0378-2222-01)
0378-2223-01 0378-2223 HUMAN PRESCRIPTION DRUG Nisoldipine Nisoldipine TABLET, FILM COATED, EXTENDED RELEASE ORAL 20080725 20300101 ANDA ANDA079051 Mylan Pharmaceuticals Inc. NISOLDIPINE 30 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0378-2223-01)
0378-2224-01 0378-2224 HUMAN PRESCRIPTION DRUG Nisoldipine Nisoldipine TABLET, FILM COATED, EXTENDED RELEASE ORAL 20080725 20300101 ANDA ANDA079051 Mylan Pharmaceuticals Inc. NISOLDIPINE 40 mg/1 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0378-2224-01)
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