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=ANDA206530"
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
65862-860-05 65862-860 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20151222 N/A ANDA ANDA206530 Aurobindo Pharma Limited FAMOTIDINE 40 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (65862-860-05)
65862-860-30 65862-860 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20151222 N/A ANDA ANDA206530 Aurobindo Pharma Limited FAMOTIDINE 40 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (65862-860-30)
65862-860-78 65862-860 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20151222 N/A ANDA ANDA206530 Aurobindo Pharma Limited FAMOTIDINE 40 mg/1 10 BLISTER PACK in 1 CARTON (65862-860-78) / 10 TABLET, FILM COATED in 1 BLISTER PACK (65862-860-10)
65862-860-99 65862-860 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20151222 N/A ANDA ANDA206530 Aurobindo Pharma Limited FAMOTIDINE 40 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (65862-860-99)
71335-0370-1 71335-0370 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20210416 N/A ANDA ANDA206530 Bryant Ranch Prepack FAMOTIDINE 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71335-0370-1)
71335-0370-2 71335-0370 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20210723 N/A ANDA ANDA206530 Bryant Ranch Prepack FAMOTIDINE 20 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71335-0370-2)
71335-0370-3 71335-0370 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20211227 N/A ANDA ANDA206530 Bryant Ranch Prepack FAMOTIDINE 20 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (71335-0370-3)
71335-0370-4 71335-0370 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20210504 N/A ANDA ANDA206530 Bryant Ranch Prepack FAMOTIDINE 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71335-0370-4)
71335-0370-5 71335-0370 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20211227 N/A ANDA ANDA206530 Bryant Ranch Prepack FAMOTIDINE 20 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (71335-0370-5)
71335-0370-6 71335-0370 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20210629 N/A ANDA ANDA206530 Bryant Ranch Prepack FAMOTIDINE 20 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (71335-0370-6)
71335-0370-7 71335-0370 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20210902 N/A ANDA ANDA206530 Bryant Ranch Prepack FAMOTIDINE 20 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (71335-0370-7)
71335-0370-8 71335-0370 HUMAN PRESCRIPTION DRUG Famotidine Famotidine TABLET, FILM COATED ORAL 20211227 N/A ANDA ANDA206530 Bryant Ranch Prepack FAMOTIDINE 20 mg/1 50 TABLET, FILM COATED in 1 BOTTLE (71335-0370-8)
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