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
68071-3509-6	68071-3509	HUMAN PRESCRIPTION DRUG	PHENDIMETRAZINE TARTRATE	Phendimetrazine Tartrate	TABLET	ORAL	20230919	N/A	ANDA	ANDA040762	NuCare Pharmaceuticals,Inc.	PHENDIMETRAZINE TARTRATE	35 mg/1	60 TABLET in 1 BOTTLE (68071-3509-6)
68071-3509-9	68071-3509	HUMAN PRESCRIPTION DRUG	PHENDIMETRAZINE TARTRATE	Phendimetrazine Tartrate	TABLET	ORAL	20230919	N/A	ANDA	ANDA040762	NuCare Pharmaceuticals,Inc.	PHENDIMETRAZINE TARTRATE	35 mg/1	90 TABLET in 1 BOTTLE (68071-3509-9)
72162-2044-0	72162-2044	HUMAN PRESCRIPTION DRUG	PHENDIMETRAZINE TARTRATE	Phendimetrazine Tartrate	TABLET	ORAL	20230614	N/A	ANDA	ANDA040762	Bryant Ranch Prepack	PHENDIMETRAZINE TARTRATE	35 mg/1	1000 TABLET in 1 BOTTLE (72162-2044-0)
72162-2044-1	72162-2044	HUMAN PRESCRIPTION DRUG	PHENDIMETRAZINE TARTRATE	Phendimetrazine Tartrate	TABLET	ORAL	20230614	N/A	ANDA	ANDA040762	Bryant Ranch Prepack	PHENDIMETRAZINE TARTRATE	35 mg/1	100 TABLET in 1 BOTTLE (72162-2044-1)
72162-2044-3	72162-2044	HUMAN PRESCRIPTION DRUG	PHENDIMETRAZINE TARTRATE	Phendimetrazine Tartrate	TABLET	ORAL	20230614	N/A	ANDA	ANDA040762	Bryant Ranch Prepack	PHENDIMETRAZINE TARTRATE	35 mg/1	30 TABLET in 1 BOTTLE (72162-2044-3)
72162-2044-6	72162-2044	HUMAN PRESCRIPTION DRUG	PHENDIMETRAZINE TARTRATE	Phendimetrazine Tartrate	TABLET	ORAL	20230614	N/A	ANDA	ANDA040762	Bryant Ranch Prepack	PHENDIMETRAZINE TARTRATE	35 mg/1	60 TABLET in 1 BOTTLE (72162-2044-6)
64850-440-01	64850-440	HUMAN PRESCRIPTION DRUG	PHENDIMETRAZINE TARTRATE	Phendimetrazine Tartrate	TABLET	ORAL	20121120	N/A	ANDA	ANDA040762	Elite Laboratories, Inc	PHENDIMETRAZINE TARTRATE	35 mg/1	100 TABLET in 1 BOTTLE (64850-440-01)
64850-440-10	64850-440	HUMAN PRESCRIPTION DRUG	PHENDIMETRAZINE TARTRATE	Phendimetrazine Tartrate	TABLET	ORAL	20121120	N/A	ANDA	ANDA040762	Elite Laboratories, Inc	PHENDIMETRAZINE TARTRATE	35 mg/1	1000 TABLET in 1 BOTTLE (64850-440-10)