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=ANDA204359"
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
69844-036-04 69844-036 HUMAN PRESCRIPTION DRUG CLOPIDOGREL BISULFATE CLOPIDOGREL BISULFATE TABLET ORAL 20200406 N/A ANDA ANDA204359 Graviti Pharmaceuticals Private Limited CLOPIDOGREL BISULFATE 75 mg/1 1000 TABLET in 1 BOTTLE (69844-036-04)
69844-036-03 69844-036 HUMAN PRESCRIPTION DRUG CLOPIDOGREL BISULFATE CLOPIDOGREL BISULFATE TABLET ORAL 20200406 N/A ANDA ANDA204359 Graviti Pharmaceuticals Private Limited CLOPIDOGREL BISULFATE 75 mg/1 500 TABLET in 1 BOTTLE (69844-036-03)
69844-036-02 69844-036 HUMAN PRESCRIPTION DRUG CLOPIDOGREL BISULFATE CLOPIDOGREL BISULFATE TABLET ORAL 20200406 N/A ANDA ANDA204359 Graviti Pharmaceuticals Private Limited CLOPIDOGREL BISULFATE 75 mg/1 90 TABLET in 1 BOTTLE (69844-036-02)
69844-036-01 69844-036 HUMAN PRESCRIPTION DRUG CLOPIDOGREL BISULFATE CLOPIDOGREL BISULFATE TABLET ORAL 20200406 N/A ANDA ANDA204359 Graviti Pharmaceuticals Private Limited CLOPIDOGREL BISULFATE 75 mg/1 30 TABLET in 1 BOTTLE (69844-036-01)
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