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=ANDA076273"
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
55111-196-01 55111-196 HUMAN PRESCRIPTION DRUG Clopidogrel bisulfate Clopidogrel bisulfate TABLET, FILM COATED ORAL 20120517 N/A ANDA ANDA076273 Dr.Reddy's Laboratories Limited CLOPIDOGREL BISULFATE 75 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (55111-196-01)
55111-196-05 55111-196 HUMAN PRESCRIPTION DRUG Clopidogrel bisulfate Clopidogrel bisulfate TABLET, FILM COATED ORAL 20120517 N/A ANDA ANDA076273 Dr.Reddy's Laboratories Limited CLOPIDOGREL BISULFATE 75 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (55111-196-05)
55111-196-30 55111-196 HUMAN PRESCRIPTION DRUG Clopidogrel bisulfate Clopidogrel bisulfate TABLET, FILM COATED ORAL 20120517 N/A ANDA ANDA076273 Dr.Reddy's Laboratories Limited CLOPIDOGREL BISULFATE 75 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (55111-196-30)
55111-196-90 55111-196 HUMAN PRESCRIPTION DRUG Clopidogrel bisulfate Clopidogrel bisulfate TABLET, FILM COATED ORAL 20120517 N/A ANDA ANDA076273 Dr.Reddy's Laboratories Limited CLOPIDOGREL BISULFATE 75 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (55111-196-90)
82009-021-05 82009-021 HUMAN PRESCRIPTION DRUG Clopidogrel bisulfate Clopidogrel bisulfate TABLET, FILM COATED ORAL 20221115 N/A ANDA ANDA076273 Quallent Pharmaceuticals Health LLC CLOPIDOGREL BISULFATE 75 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (82009-021-05)
82009-021-90 82009-021 HUMAN PRESCRIPTION DRUG Clopidogrel bisulfate Clopidogrel bisulfate TABLET, FILM COATED ORAL 20221115 N/A ANDA ANDA076273 Quallent Pharmaceuticals Health LLC CLOPIDOGREL BISULFATE 75 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (82009-021-90)
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