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
70518-2767-1	70518-2767	HUMAN PRESCRIPTION DRUG	Mycophenolate mofetil	Mycophenolate mofetil	TABLET, FILM COATED	ORAL	20211216	N/A	ANDA	ANDA090456	REMEDYREPACK INC.	MYCOPHENOLATE MOFETIL	500 mg/1	100 POUCH in 1 BOX (70518-2767-1) / 1 TABLET, FILM COATED in 1 POUCH (70518-2767-2)
23155-836-01	23155-836	HUMAN PRESCRIPTION DRUG	Mycophenolate mofetil	Mycophenolate mofetil	TABLET, FILM COATED	ORAL	20221015	N/A	ANDA	ANDA090456	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	MYCOPHENOLATE MOFETIL	500 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (23155-836-01)
23155-836-05	23155-836	HUMAN PRESCRIPTION DRUG	Mycophenolate mofetil	Mycophenolate mofetil	TABLET, FILM COATED	ORAL	20221015	N/A	ANDA	ANDA090456	Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.	MYCOPHENOLATE MOFETIL	500 mg/1	500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (23155-836-05)
68071-3767-6	68071-3767	HUMAN PRESCRIPTION DRUG	Mycophenolate mofetil	Mycophenolate mofetil	TABLET, FILM COATED	ORAL	20250113	N/A	ANDA	ANDA090456	NuCare Pharmaceuticals, Inc.	MYCOPHENOLATE MOFETIL	500 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68071-3767-6)
64380-725-06	64380-725	HUMAN PRESCRIPTION DRUG	Mycophenolate mofetil	Mycophenolate mofetil	TABLET, FILM COATED	ORAL	20101106	N/A	ANDA	ANDA090456	Strides Pharma Science Limited	MYCOPHENOLATE MOFETIL	500 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (64380-725-06)
64380-725-07	64380-725	HUMAN PRESCRIPTION DRUG	Mycophenolate mofetil	Mycophenolate mofetil	TABLET, FILM COATED	ORAL	20101106	N/A	ANDA	ANDA090456	Strides Pharma Science Limited	MYCOPHENOLATE MOFETIL	500 mg/1	500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (64380-725-07)
73190-010-01	73190-010	HUMAN PRESCRIPTION DRUG	Mycophenolate mofetil	Mycophenolate mofetil	TABLET, FILM COATED	ORAL	20250425	N/A	ANDA	ANDA090456	AvKARE	MYCOPHENOLATE MOFETIL	500 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (73190-010-01)
73190-010-50	73190-010	HUMAN PRESCRIPTION DRUG	Mycophenolate mofetil	Mycophenolate mofetil	TABLET, FILM COATED	ORAL	20250425	N/A	ANDA	ANDA090456	AvKARE	MYCOPHENOLATE MOFETIL	500 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (73190-010-50)
70518-4377-0	70518-4377	HUMAN PRESCRIPTION DRUG	Mycophenolate mofetil	Mycophenolate mofetil	TABLET, FILM COATED	ORAL	20250630	N/A	ANDA	ANDA090456	REMEDYREPACK INC.	MYCOPHENOLATE MOFETIL	500 mg/1	100 POUCH in 1 BOX (70518-4377-0) / 1 TABLET, FILM COATED in 1 POUCH (70518-4377-1)
0904-7078-61	0904-7078	HUMAN PRESCRIPTION DRUG	Mycophenolate mofetil	Mycophenolate mofetil	TABLET, FILM COATED	ORAL	20101106	N/A	ANDA	ANDA090456	Major Pharmaceuticals	MYCOPHENOLATE MOFETIL	500 mg/1	100 BLISTER PACK in 1 CAPSULE (0904-7078-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK
55154-3571-0	55154-3571	HUMAN PRESCRIPTION DRUG	Mycophenolate mofetil	Mycophenolate mofetil	TABLET, FILM COATED	ORAL	20101106	N/A	ANDA	ANDA090456	Cardinal Health 107, LLC	MYCOPHENOLATE MOFETIL	500 mg/1	10 BLISTER PACK in 1 BAG (55154-3571-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK
82804-033-30	82804-033	HUMAN PRESCRIPTION DRUG	Mycophenolate mofetil	Mycophenolate mofetil	TABLET, FILM COATED	ORAL	20231025	N/A	ANDA	ANDA090456	Proficient Rx LP	MYCOPHENOLATE MOFETIL	500 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (82804-033-30)
82804-033-60	82804-033	HUMAN PRESCRIPTION DRUG	Mycophenolate mofetil	Mycophenolate mofetil	TABLET, FILM COATED	ORAL	20231025	N/A	ANDA	ANDA090456	Proficient Rx LP	MYCOPHENOLATE MOFETIL	500 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (82804-033-60)
82804-033-90	82804-033	HUMAN PRESCRIPTION DRUG	Mycophenolate mofetil	Mycophenolate mofetil	TABLET, FILM COATED	ORAL	20231025	N/A	ANDA	ANDA090456	Proficient Rx LP	MYCOPHENOLATE MOFETIL	500 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (82804-033-90)
60687-438-01	60687-438	HUMAN PRESCRIPTION DRUG	Mycophenolate mofetil	Mycophenolate Mofetil	TABLET, FILM COATED	ORAL	20190614	N/A	ANDA	ANDA090456	American Health Packaging	MYCOPHENOLATE MOFETIL	500 mg/1	100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-438-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-438-11)