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=ANDA076919"
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
55154-5699-0 55154-5699 HUMAN PRESCRIPTION DRUG Levetiracetam levetiracetam TABLET, FILM COATED ORAL 20120829 N/A ANDA ANDA076919 Cardinal Health 107, LLC LEVETIRACETAM 500 mg/1 10 BLISTER PACK in 1 BAG (55154-5699-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK
0378-5615-05 0378-5615 HUMAN PRESCRIPTION DRUG Levetiracetam levetiracetam TABLET, FILM COATED ORAL 20081104 N/A ANDA ANDA076919 Mylan Pharmaceuticals Inc. LEVETIRACETAM 500 mg/1 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-5615-05)
0378-5615-78 0378-5615 HUMAN PRESCRIPTION DRUG Levetiracetam levetiracetam TABLET, FILM COATED ORAL 20081104 N/A ANDA ANDA076919 Mylan Pharmaceuticals Inc. LEVETIRACETAM 500 mg/1 120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-5615-78)
0378-5617-05 0378-5617 HUMAN PRESCRIPTION DRUG Levetiracetam levetiracetam TABLET, FILM COATED ORAL 20081104 N/A ANDA ANDA076919 Mylan Pharmaceuticals Inc. LEVETIRACETAM 750 mg/1 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-5617-05)
0378-5617-78 0378-5617 HUMAN PRESCRIPTION DRUG Levetiracetam levetiracetam TABLET, FILM COATED ORAL 20081104 N/A ANDA ANDA076919 Mylan Pharmaceuticals Inc. LEVETIRACETAM 750 mg/1 120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-5617-78)
51079-821-20 51079-821 HUMAN PRESCRIPTION DRUG Levetiracetam levetiracetam TABLET, FILM COATED ORAL 20081104 N/A ANDA ANDA076919 Mylan Institutional Inc. LEVETIRACETAM 500 mg/1 100 BLISTER PACK in 1 CARTON (51079-821-20) / 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-821-01)
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