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=ANDA210568"
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
68071-3616-4 68071-3616 HUMAN PRESCRIPTION DRUG Cefpodoxime Proxetil Cefpodoxime Proxetil TABLET, FILM COATED ORAL 20240619 N/A ANDA ANDA210568 NuCare Pharmaceuticals,Inc. CEFPODOXIME PROXETIL 100 mg/1 14 TABLET, FILM COATED in 1 BOTTLE (68071-3616-4)
69292-510-01 69292-510 HUMAN PRESCRIPTION DRUG Cefpodoxime Proxetil Cefpodoxime Proxetil TABLET, FILM COATED ORAL 20220826 N/A ANDA ANDA210568 Amici Pharmaceuticals, LLC. CEFPODOXIME PROXETIL 100 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (69292-510-01)
69292-510-50 69292-510 HUMAN PRESCRIPTION DRUG Cefpodoxime Proxetil Cefpodoxime Proxetil TABLET, FILM COATED ORAL 20220826 N/A ANDA ANDA210568 Amici Pharmaceuticals, LLC. CEFPODOXIME PROXETIL 100 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (69292-510-50)
68071-3441-2 68071-3441 HUMAN PRESCRIPTION DRUG Cefpodoxime Proxetil Cefpodoxime Proxetil TABLET, FILM COATED ORAL 20230619 N/A ANDA ANDA210568 NuCare Pharmaceuticals,Inc. CEFPODOXIME PROXETIL 200 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (68071-3441-2)
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