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
72205-139-28	72205-139	HUMAN PRESCRIPTION DRUG	Tofacitinib	Tofacitinib	TABLET, FILM COATED	ORAL	20260603	N/A	ANDA	ANDA217299	Novadoz Pharmaceuticals LLC	TOFACITINIB CITRATE	5 mg/1	28 TABLET, FILM COATED in 1 BOTTLE (72205-139-28)
72205-139-60	72205-139	HUMAN PRESCRIPTION DRUG	Tofacitinib	Tofacitinib	TABLET, FILM COATED	ORAL	20260603	N/A	ANDA	ANDA217299	Novadoz Pharmaceuticals LLC	TOFACITINIB CITRATE	5 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (72205-139-60)
72205-140-18	72205-140	HUMAN PRESCRIPTION DRUG	Tofacitinib	Tofacitinib	TABLET, FILM COATED	ORAL	20260603	N/A	ANDA	ANDA217299	Novadoz Pharmaceuticals LLC	TOFACITINIB CITRATE	10 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (72205-140-18)
72205-140-28	72205-140	HUMAN PRESCRIPTION DRUG	Tofacitinib	Tofacitinib	TABLET, FILM COATED	ORAL	20260603	N/A	ANDA	ANDA217299	Novadoz Pharmaceuticals LLC	TOFACITINIB CITRATE	10 mg/1	28 TABLET, FILM COATED in 1 BOTTLE (72205-140-28)
72205-140-60	72205-140	HUMAN PRESCRIPTION DRUG	Tofacitinib	Tofacitinib	TABLET, FILM COATED	ORAL	20260603	N/A	ANDA	ANDA217299	Novadoz Pharmaceuticals LLC	TOFACITINIB CITRATE	10 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (72205-140-60)