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=ANDA213055"
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
70771-1595-1 70771-1595 HUMAN PRESCRIPTION DRUG Midodrine hydrochloride Midodrine hydrochloride TABLET ORAL 20200917 N/A ANDA ANDA213055 Zydus Lifesciences Limited MIDODRINE HYDROCHLORIDE 2.5 mg/1 100 TABLET in 1 BOTTLE (70771-1595-1)
68382-739-01 68382-739 HUMAN PRESCRIPTION DRUG Midodrine hydrochloride Midodrine hydrochloride TABLET ORAL 20200917 N/A ANDA ANDA213055 Zydus Pharmaceuticals (USA) Inc. MIDODRINE HYDROCHLORIDE 10 mg/1 100 TABLET in 1 BOTTLE (68382-739-01)
68382-738-01 68382-738 HUMAN PRESCRIPTION DRUG Midodrine hydrochloride Midodrine hydrochloride TABLET ORAL 20200917 N/A ANDA ANDA213055 Zydus Pharmaceuticals (USA) Inc. MIDODRINE HYDROCHLORIDE 5 mg/1 100 TABLET in 1 BOTTLE (68382-738-01)
70771-1597-1 70771-1597 HUMAN PRESCRIPTION DRUG Midodrine hydrochloride Midodrine hydrochloride TABLET ORAL 20200917 N/A ANDA ANDA213055 Zydus Lifesciences Limited MIDODRINE HYDROCHLORIDE 10 mg/1 100 TABLET in 1 BOTTLE (70771-1597-1)
68382-737-01 68382-737 HUMAN PRESCRIPTION DRUG Midodrine hydrochloride Midodrine hydrochloride TABLET ORAL 20200917 N/A ANDA ANDA213055 Zydus Pharmaceuticals (USA) Inc. MIDODRINE HYDROCHLORIDE 2.5 mg/1 100 TABLET in 1 BOTTLE (68382-737-01)
70771-1596-1 70771-1596 HUMAN PRESCRIPTION DRUG Midodrine hydrochloride Midodrine hydrochloride TABLET ORAL 20200917 N/A ANDA ANDA213055 Zydus Lifesciences Limited MIDODRINE HYDROCHLORIDE 5 mg/1 100 TABLET in 1 BOTTLE (70771-1596-1)
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