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）

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
55289-393-02	55289-393	HUMAN PRESCRIPTION DRUG	CEFPODOXIME PROXETIL	CEFPODOXIME PROXETIL	TABLET, FILM COATED	ORAL	20100623	N/A	ANDA	ANDA065370	PD-Rx Pharmaceuticals, Inc.	CEFPODOXIME PROXETIL	200 mg/1	2 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (55289-393-02)
16714-395-01	16714-395	HUMAN PRESCRIPTION DRUG	CEFPODOXIME PROXETIL	CEFPODOXIME PROXETIL	TABLET, FILM COATED	ORAL	20070611	N/A	ANDA	ANDA065370	NorthStar Rx LLC	CEFPODOXIME PROXETIL	200 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (16714-395-01)
16714-394-01	16714-394	HUMAN PRESCRIPTION DRUG	CEFPODOXIME PROXETIL	CEFPODOXIME PROXETIL	TABLET, FILM COATED	ORAL	20070611	N/A	ANDA	ANDA065370	NorthStar Rx LLC	CEFPODOXIME PROXETIL	100 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (16714-394-01)
69043-007-01	69043-007	HUMAN PRESCRIPTION DRUG	CEFPODOXIME PROXETIL	CEFPODOXIME PROXETIL	TABLET, FILM COATED	ORAL	20070611	N/A	ANDA	ANDA065370	Cronus Pharma LLC	CEFPODOXIME PROXETIL	200 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (69043-007-01)
69043-007-25	69043-007	HUMAN PRESCRIPTION DRUG	CEFPODOXIME PROXETIL	CEFPODOXIME PROXETIL	TABLET, FILM COATED	ORAL	20231006	N/A	ANDA	ANDA065370	Cronus Pharma LLC	CEFPODOXIME PROXETIL	200 mg/1	250 TABLET, FILM COATED in 1 BOTTLE (69043-007-25)
69043-006-01	69043-006	HUMAN PRESCRIPTION DRUG	CEFPODOXIME PROXETIL	CEFPODOXIME PROXETIL	TABLET, FILM COATED	ORAL	20070611	N/A	ANDA	ANDA065370	Cronus Pharma LLC	CEFPODOXIME PROXETIL	100 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (69043-006-01)
69043-006-25	69043-006	HUMAN PRESCRIPTION DRUG	CEFPODOXIME PROXETIL	CEFPODOXIME PROXETIL	TABLET, FILM COATED	ORAL	20231006	N/A	ANDA	ANDA065370	Cronus Pharma LLC	CEFPODOXIME PROXETIL	100 mg/1	250 TABLET, FILM COATED in 1 BOTTLE (69043-006-25)
68071-2742-1	68071-2742	HUMAN PRESCRIPTION DRUG	CEFPODOXIME PROXETIL	CEFPODOXIME PROXETIL	TABLET, FILM COATED	ORAL	20220602	N/A	ANDA	ANDA065370	NuCare Pharmaceuticals,Inc.	CEFPODOXIME PROXETIL	100 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (68071-2742-1)
65862-095-99	65862-095	HUMAN PRESCRIPTION DRUG	CEFPODOXIME PROXETIL	CEFPODOXIME PROXETIL	TABLET, FILM COATED	ORAL	20070611	N/A	ANDA	ANDA065370	Aurobindo Pharma Limited	CEFPODOXIME PROXETIL	100 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (65862-095-99)
65862-096-01	65862-096	HUMAN PRESCRIPTION DRUG	CEFPODOXIME PROXETIL	CEFPODOXIME PROXETIL	TABLET, FILM COATED	ORAL	20070611	N/A	ANDA	ANDA065370	Aurobindo Pharma Limited	CEFPODOXIME PROXETIL	200 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (65862-096-01)
65862-095-01	65862-095	HUMAN PRESCRIPTION DRUG	CEFPODOXIME PROXETIL	CEFPODOXIME PROXETIL	TABLET, FILM COATED	ORAL	20070611	N/A	ANDA	ANDA065370	Aurobindo Pharma Limited	CEFPODOXIME PROXETIL	100 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (65862-095-01)
65862-095-20	65862-095	HUMAN PRESCRIPTION DRUG	CEFPODOXIME PROXETIL	CEFPODOXIME PROXETIL	TABLET, FILM COATED	ORAL	20070611	N/A	ANDA	ANDA065370	Aurobindo Pharma Limited	CEFPODOXIME PROXETIL	100 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (65862-095-20)
65862-095-25	65862-095	HUMAN PRESCRIPTION DRUG	CEFPODOXIME PROXETIL	CEFPODOXIME PROXETIL	TABLET, FILM COATED	ORAL	20231006	N/A	ANDA	ANDA065370	Aurobindo Pharma Limited	CEFPODOXIME PROXETIL	100 mg/1	250 TABLET, FILM COATED in 1 BOTTLE (65862-095-25)
65862-096-20	65862-096	HUMAN PRESCRIPTION DRUG	CEFPODOXIME PROXETIL	CEFPODOXIME PROXETIL	TABLET, FILM COATED	ORAL	20070611	N/A	ANDA	ANDA065370	Aurobindo Pharma Limited	CEFPODOXIME PROXETIL	200 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (65862-096-20)
65862-096-25	65862-096	HUMAN PRESCRIPTION DRUG	CEFPODOXIME PROXETIL	CEFPODOXIME PROXETIL	TABLET, FILM COATED	ORAL	20231006	N/A	ANDA	ANDA065370	Aurobindo Pharma Limited	CEFPODOXIME PROXETIL	200 mg/1	250 TABLET, FILM COATED in 1 BOTTLE (65862-096-25)
65862-096-99	65862-096	HUMAN PRESCRIPTION DRUG	CEFPODOXIME PROXETIL	CEFPODOXIME PROXETIL	TABLET, FILM COATED	ORAL	20070611	N/A	ANDA	ANDA065370	Aurobindo Pharma Limited	CEFPODOXIME PROXETIL	200 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (65862-096-99)