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=ANDA073283"
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
0093-0308-01 0093-0308 HUMAN PRESCRIPTION DRUG Clemastine Fumarate Clemastine Fumarate TABLET ORAL 19920401 20260331 ANDA ANDA073283 Teva Pharmaceuticals USA, Inc. CLEMASTINE FUMARATE 2.68 mg/1 100 TABLET in 1 BOTTLE (0093-0308-01)
64950-268-03 64950-268 HUMAN PRESCRIPTION DRUG Clemastine Fumarate Clemastine Fumarate TABLET ORAL 20241120 N/A ANDA ANDA073283 Genus Lifesciences CLEMASTINE FUMARATE 2.68 mg/1 30 TABLET in 1 BOTTLE (64950-268-03)
64950-268-10 64950-268 HUMAN PRESCRIPTION DRUG Clemastine Fumarate Clemastine Fumarate TABLET ORAL 20241120 N/A ANDA ANDA073283 Genus Lifesciences CLEMASTINE FUMARATE 2.68 mg/1 100 TABLET in 1 BOTTLE (64950-268-10)
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