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=ANDA205927"
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
0378-5186-93 0378-5186 HUMAN PRESCRIPTION DRUG Prasugrel Prasugrel TABLET, FILM COATED ORAL 20170815 N/A ANDA ANDA205927 Mylan Pharmaceuticals Inc. PRASUGREL HYDROCHLORIDE 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-5186-93)
0378-5185-93 0378-5185 HUMAN PRESCRIPTION DRUG Prasugrel Prasugrel TABLET, FILM COATED ORAL 20170816 N/A ANDA ANDA205927 Mylan Pharmaceuticals Inc. PRASUGREL HYDROCHLORIDE 5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-5185-93)
51407-445-30 51407-445 HUMAN PRESCRIPTION DRUG Prasugrel Prasugrel TABLET, FILM COATED ORAL 20210120 N/A ANDA ANDA205927 Golden State Medical Supply, Inc. PRASUGREL HYDROCHLORIDE 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51407-445-30)
51407-444-30 51407-444 HUMAN PRESCRIPTION DRUG Prasugrel Prasugrel TABLET, FILM COATED ORAL 20210120 N/A ANDA ANDA205927 Golden State Medical Supply, Inc. PRASUGREL HYDROCHLORIDE 5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51407-444-30)
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