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
82009-086-90	82009-086	HUMAN PRESCRIPTION DRUG	Imatinib Mesylate	Imatinib Mesylate	TABLET, FILM COATED	ORAL	20230901	N/A	ANDA	ANDA212773	QUALLENT PHARMACEUTICALS HEALTH LLC	IMATINIB MESYLATE	100 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (82009-086-90)
82009-087-30	82009-087	HUMAN PRESCRIPTION DRUG	Imatinib Mesylate	Imatinib Mesylate	TABLET, FILM COATED	ORAL	20230901	N/A	ANDA	ANDA212773	QUALLENT PHARMACEUTICALS HEALTH LLC	IMATINIB MESYLATE	400 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (82009-087-30)
68001-622-05	68001-622	HUMAN PRESCRIPTION DRUG	Imatinib Mesylate	Imatinib Mesylate	TABLET, FILM COATED	ORAL	20250305	N/A	ANDA	ANDA212773	BluePoint Laboratories	IMATINIB MESYLATE	100 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68001-622-05)
59651-240-90	59651-240	HUMAN PRESCRIPTION DRUG	Imatinib Mesylate	Imatinib Mesylate	TABLET, FILM COATED	ORAL	20200723	N/A	ANDA	ANDA212773	Aurobindo Pharma Limited	IMATINIB MESYLATE	100 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (59651-240-90)
68001-623-04	68001-623	HUMAN PRESCRIPTION DRUG	Imatinib Mesylate	Imatinib Mesylate	TABLET, FILM COATED	ORAL	20250221	N/A	ANDA	ANDA212773	BluePoint Laboratories	IMATINIB MESYLATE	400 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68001-623-04)
59651-241-03	59651-241	HUMAN PRESCRIPTION DRUG	Imatinib Mesylate	Imatinib Mesylate	TABLET, FILM COATED	ORAL	20200723	N/A	ANDA	ANDA212773	Aurobindo Pharma Limited	IMATINIB MESYLATE	400 mg/1	3 BLISTER PACK in 1 CARTON (59651-241-03) / 10 TABLET, FILM COATED in 1 BLISTER PACK
59651-241-30	59651-241	HUMAN PRESCRIPTION DRUG	Imatinib Mesylate	Imatinib Mesylate	TABLET, FILM COATED	ORAL	20200723	N/A	ANDA	ANDA212773	Aurobindo Pharma Limited	IMATINIB MESYLATE	400 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (59651-241-30)