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=ANDA207175"
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
42658-149-03 42658-149 HUMAN PRESCRIPTION DRUG LEVETIRACETAM LEVETIRACETAM TABLET, FILM COATED, EXTENDED RELEASE ORAL 20250101 N/A ANDA ANDA207175 Hisun Pharmaceuticals USA, Inc. LEVETIRACETAM 750 mg/1 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42658-149-03)
42658-149-07 42658-149 HUMAN PRESCRIPTION DRUG LEVETIRACETAM LEVETIRACETAM TABLET, FILM COATED, EXTENDED RELEASE ORAL 20250101 N/A ANDA ANDA207175 Hisun Pharmaceuticals USA, Inc. LEVETIRACETAM 750 mg/1 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42658-149-07)
42658-148-03 42658-148 HUMAN PRESCRIPTION DRUG LEVETIRACETAM LEVETIRACETAM TABLET, FILM COATED, EXTENDED RELEASE ORAL 20250101 N/A ANDA ANDA207175 Hisun Pharmaceuticals USA, Inc. LEVETIRACETAM 500 mg/1 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42658-148-03)
42658-148-07 42658-148 HUMAN PRESCRIPTION DRUG LEVETIRACETAM LEVETIRACETAM TABLET, FILM COATED, EXTENDED RELEASE ORAL 20250101 N/A ANDA ANDA207175 Hisun Pharmaceuticals USA, Inc. LEVETIRACETAM 500 mg/1 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42658-148-07)
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