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=ANDA206015"
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
65862-813-90 65862-813 HUMAN PRESCRIPTION DRUG Pitavastatin Pitavastatin TABLET, FILM COATED ORAL 20231102 N/A ANDA ANDA206015 Aurobindo Pharma Limited PITAVASTATIN CALCIUM 2 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (65862-813-90)
65862-814-05 65862-814 HUMAN PRESCRIPTION DRUG Pitavastatin Pitavastatin TABLET, FILM COATED ORAL 20231102 N/A ANDA ANDA206015 Aurobindo Pharma Limited PITAVASTATIN CALCIUM 4 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (65862-814-05)
65862-814-90 65862-814 HUMAN PRESCRIPTION DRUG Pitavastatin Pitavastatin TABLET, FILM COATED ORAL 20231102 N/A ANDA ANDA206015 Aurobindo Pharma Limited PITAVASTATIN CALCIUM 4 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (65862-814-90)
65862-813-05 65862-813 HUMAN PRESCRIPTION DRUG Pitavastatin Pitavastatin TABLET, FILM COATED ORAL 20231102 N/A ANDA ANDA206015 Aurobindo Pharma Limited PITAVASTATIN CALCIUM 2 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (65862-813-05)
65862-812-90 65862-812 HUMAN PRESCRIPTION DRUG Pitavastatin Pitavastatin TABLET, FILM COATED ORAL 20231102 N/A ANDA ANDA206015 Aurobindo Pharma Limited PITAVASTATIN CALCIUM 1 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (65862-812-90)
65862-812-05 65862-812 HUMAN PRESCRIPTION DRUG Pitavastatin Pitavastatin TABLET, FILM COATED ORAL 20231102 N/A ANDA ANDA206015 Aurobindo Pharma Limited PITAVASTATIN CALCIUM 1 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (65862-812-05)
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