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=ANDA217878"
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
70010-522-10 70010-522 HUMAN PRESCRIPTION DRUG Levetiracetam Levetiracetam TABLET, FILM COATED ORAL 20240624 N/A ANDA ANDA217878 Granules Pharmaceuticals Inc. LEVETIRACETAM 500 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (70010-522-10)
70010-523-03 70010-523 HUMAN PRESCRIPTION DRUG Levetiracetam Levetiracetam TABLET, FILM COATED ORAL 20240624 N/A ANDA ANDA217878 Granules Pharmaceuticals Inc. LEVETIRACETAM 750 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (70010-523-03)
70010-523-10 70010-523 HUMAN PRESCRIPTION DRUG Levetiracetam Levetiracetam TABLET, FILM COATED ORAL 20240624 N/A ANDA ANDA217878 Granules Pharmaceuticals Inc. LEVETIRACETAM 750 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (70010-523-10)
70010-524-03 70010-524 HUMAN PRESCRIPTION DRUG Levetiracetam Levetiracetam TABLET, FILM COATED ORAL 20240624 N/A ANDA ANDA217878 Granules Pharmaceuticals Inc. LEVETIRACETAM 1000 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (70010-524-03)
70010-524-10 70010-524 HUMAN PRESCRIPTION DRUG Levetiracetam Levetiracetam TABLET, FILM COATED ORAL 20240624 N/A ANDA ANDA217878 Granules Pharmaceuticals Inc. LEVETIRACETAM 1000 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (70010-524-10)
70010-522-03 70010-522 HUMAN PRESCRIPTION DRUG Levetiracetam Levetiracetam TABLET, FILM COATED ORAL 20240624 N/A ANDA ANDA217878 Granules Pharmaceuticals Inc. LEVETIRACETAM 500 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (70010-522-03)
70010-521-10 70010-521 HUMAN PRESCRIPTION DRUG Levetiracetam Levetiracetam TABLET, FILM COATED ORAL 20240624 N/A ANDA ANDA217878 Granules Pharmaceuticals Inc. LEVETIRACETAM 250 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (70010-521-10)
70010-521-03 70010-521 HUMAN PRESCRIPTION DRUG Levetiracetam Levetiracetam TABLET, FILM COATED ORAL 20240624 N/A ANDA ANDA217878 Granules Pharmaceuticals Inc. LEVETIRACETAM 250 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (70010-521-03)
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