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=ANDA215388"
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
72205-199-01 72205-199 HUMAN PRESCRIPTION DRUG CLOPIDOGREL CLOPIDOGREL BISULFATE TABLET, FILM COATED ORAL 20251112 N/A ANDA ANDA215388 Novadoz Pharmaceuticals LLC CLOPIDOGREL BISULFATE 75 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (72205-199-01)
72205-199-05 72205-199 HUMAN PRESCRIPTION DRUG CLOPIDOGREL CLOPIDOGREL BISULFATE TABLET, FILM COATED ORAL 20241122 N/A ANDA ANDA215388 Novadoz Pharmaceuticals LLC CLOPIDOGREL BISULFATE 75 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (72205-199-05)
72205-199-06 72205-199 HUMAN PRESCRIPTION DRUG CLOPIDOGREL CLOPIDOGREL BISULFATE TABLET, FILM COATED ORAL 20241122 N/A ANDA ANDA215388 Novadoz Pharmaceuticals LLC CLOPIDOGREL BISULFATE 75 mg/1 10 BLISTER PACK in 1 CARTON (72205-199-06) / 10 TABLET, FILM COATED in 1 BLISTER PACK (72205-199-11)
72205-199-30 72205-199 HUMAN PRESCRIPTION DRUG CLOPIDOGREL CLOPIDOGREL BISULFATE TABLET, FILM COATED ORAL 20241122 N/A ANDA ANDA215388 Novadoz Pharmaceuticals LLC CLOPIDOGREL BISULFATE 75 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (72205-199-30)
72205-199-90 72205-199 HUMAN PRESCRIPTION DRUG CLOPIDOGREL CLOPIDOGREL BISULFATE TABLET, FILM COATED ORAL 20241122 N/A ANDA ANDA215388 Novadoz Pharmaceuticals LLC CLOPIDOGREL BISULFATE 75 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (72205-199-90)
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