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=ANDA212688"
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
81665-101-12 81665-101 HUMAN PRESCRIPTION DRUG LEVETIRACETAM Extended-release LEVETIRACETAM TABLET, EXTENDED RELEASE ORAL 20230505 N/A ANDA ANDA212688 Omnivium Pharmaceuticals LLC LEVETIRACETAM 500 mg/1 120 TABLET, EXTENDED RELEASE in 1 BOTTLE (81665-101-12)
81665-101-60 81665-101 HUMAN PRESCRIPTION DRUG LEVETIRACETAM Extended-release LEVETIRACETAM TABLET, EXTENDED RELEASE ORAL 20230505 N/A ANDA ANDA212688 Omnivium Pharmaceuticals LLC LEVETIRACETAM 500 mg/1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (81665-101-60)
81665-100-12 81665-100 HUMAN PRESCRIPTION DRUG LEVETIRACETAM Extended-release LEVETIRACETAM TABLET, EXTENDED RELEASE ORAL 20221024 N/A ANDA ANDA212688 Omnivium Pharmaceuticals LLC LEVETIRACETAM 750 mg/1 120 TABLET, EXTENDED RELEASE in 1 BOTTLE (81665-100-12)
81665-100-60 81665-100 HUMAN PRESCRIPTION DRUG LEVETIRACETAM Extended-release LEVETIRACETAM TABLET, EXTENDED RELEASE ORAL 20200611 N/A ANDA ANDA212688 Omnivium Pharmaceuticals LLC LEVETIRACETAM 750 mg/1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (81665-100-60)
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