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
70771-1628-3	70771-1628	HUMAN PRESCRIPTION DRUG	tofacitinib	tofacitinib	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20260520	N/A	ANDA	ANDA214264	Zydus Lifesciences Limited	TOFACITINIB CITRATE	22 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70771-1628-3)
70771-1628-9	70771-1628	HUMAN PRESCRIPTION DRUG	tofacitinib	tofacitinib	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20260520	N/A	ANDA	ANDA214264	Zydus Lifesciences Limited	TOFACITINIB CITRATE	22 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70771-1628-9)
70710-1353-3	70710-1353	HUMAN PRESCRIPTION DRUG	tofacitinib	tofacitinib	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20260520	N/A	ANDA	ANDA214264	Zydus Pharmaceuticals USA Inc.	TOFACITINIB CITRATE	11 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70710-1353-3)
70710-1353-9	70710-1353	HUMAN PRESCRIPTION DRUG	tofacitinib	tofacitinib	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20260520	N/A	ANDA	ANDA214264	Zydus Pharmaceuticals USA Inc.	TOFACITINIB CITRATE	11 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70710-1353-9)
70771-1627-3	70771-1627	HUMAN PRESCRIPTION DRUG	tofacitinib	tofacitinib	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20260520	N/A	ANDA	ANDA214264	Zydus Lifesciences Limited	TOFACITINIB CITRATE	11 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70771-1627-3)
70771-1627-9	70771-1627	HUMAN PRESCRIPTION DRUG	tofacitinib	tofacitinib	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20260520	N/A	ANDA	ANDA214264	Zydus Lifesciences Limited	TOFACITINIB CITRATE	11 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70771-1627-9)
70710-1727-3	70710-1727	HUMAN PRESCRIPTION DRUG	tofacitinib	tofacitinib	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20260520	N/A	ANDA	ANDA214264	Zydus Pharmaceuticals USA Inc.	TOFACITINIB CITRATE	22 mg/1	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70710-1727-3)
70710-1727-9	70710-1727	HUMAN PRESCRIPTION DRUG	tofacitinib	tofacitinib	TABLET, FILM COATED, EXTENDED RELEASE	ORAL	20260520	N/A	ANDA	ANDA214264	Zydus Pharmaceuticals USA Inc.	TOFACITINIB CITRATE	22 mg/1	90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (70710-1727-9)