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)
检索条件:" 注册申请号=ANDA090456"
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
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)
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)
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)
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
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)
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