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
42571-268-05	42571-268	HUMAN PRESCRIPTION DRUG	TOFACITINIB	tofacitinib	TABLET, FILM COATED	ORAL	20260603	N/A	ANDA	ANDA209738	Micro Labs Limited	TOFACITINIB CITRATE	5 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (42571-268-05)
42571-268-30	42571-268	HUMAN PRESCRIPTION DRUG	TOFACITINIB	tofacitinib	TABLET, FILM COATED	ORAL	20260603	N/A	ANDA	ANDA209738	Micro Labs Limited	TOFACITINIB CITRATE	5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (42571-268-30)
42571-268-60	42571-268	HUMAN PRESCRIPTION DRUG	TOFACITINIB	tofacitinib	TABLET, FILM COATED	ORAL	20260603	N/A	ANDA	ANDA209738	Micro Labs Limited	TOFACITINIB CITRATE	5 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (42571-268-60)
42571-268-76	42571-268	HUMAN PRESCRIPTION DRUG	TOFACITINIB	tofacitinib	TABLET, FILM COATED	ORAL	20260603	N/A	ANDA	ANDA209738	Micro Labs Limited	TOFACITINIB CITRATE	5 mg/1	150 BLISTER PACK in 1 CARTON (42571-268-76) / 15 TABLET, FILM COATED in 1 BLISTER PACK (42571-268-13)
42571-377-05	42571-377	HUMAN PRESCRIPTION DRUG	TOFACITINIB	tofacitinib	TABLET, FILM COATED	ORAL	20260608	N/A	ANDA	ANDA209738	Micro Labs Limited	TOFACITINIB CITRATE	10 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (42571-377-05)
42571-377-30	42571-377	HUMAN PRESCRIPTION DRUG	TOFACITINIB	tofacitinib	TABLET, FILM COATED	ORAL	20260608	N/A	ANDA	ANDA209738	Micro Labs Limited	TOFACITINIB CITRATE	10 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (42571-377-30)
42571-377-60	42571-377	HUMAN PRESCRIPTION DRUG	TOFACITINIB	tofacitinib	TABLET, FILM COATED	ORAL	20260608	N/A	ANDA	ANDA209738	Micro Labs Limited	TOFACITINIB CITRATE	10 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (42571-377-60)
42571-377-76	42571-377	HUMAN PRESCRIPTION DRUG	TOFACITINIB	tofacitinib	TABLET, FILM COATED	ORAL	20260608	N/A	ANDA	ANDA209738	Micro Labs Limited	TOFACITINIB CITRATE	10 mg/1	150 BLISTER PACK in 1 CARTON (42571-377-76) / 15 TABLET, FILM COATED in 1 BLISTER PACK (42571-377-13)