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=ANDA078947"
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
69102-320-01 69102-320 HUMAN PRESCRIPTION DRUG SUBVENITE LAMOTRIGINE TABLET ORAL 20180310 N/A ANDA ANDA078947 OWP Pharmaceuticals, Inc. LAMOTRIGINE 200 mg/1 100 TABLET in 1 BOTTLE (69102-320-01)
69102-150-06 69102-150 HUMAN PRESCRIPTION DRUG SUBVENITE LAMOTRIGINE TABLET ORAL 20180310 N/A ANDA ANDA078947 OWP Pharmaceuticals, Inc. LAMOTRIGINE 150 mg/1 100 TABLET in 1 BOTTLE (69102-150-06)
69102-312-01 69102-312 HUMAN PRESCRIPTION DRUG SUBVENITE LAMOTRIGINE KIT 20180414 N/A ANDA ANDA078947 OWP Pharmaceuticals, Inc. 14 BLISTER PACK in 1 PACKAGE, COMBINATION (69102-312-01) / 1 KIT in 1 BLISTER PACK
69102-639-09 69102-639 HUMAN PRESCRIPTION DRUG LAMOTRIGINE LAMOTRIGINE TABLET ORAL 20170830 N/A ANDA ANDA078947 OWP Pharmaceuticals, Inc. LAMOTRIGINE 25 mg/1 35 TABLET in 1 DOSE PACK (69102-639-09)
69102-300-01 69102-300 HUMAN PRESCRIPTION DRUG SUBVENITE LAMOTRIGINE KIT 20180414 N/A ANDA ANDA078947 OWP Pharmaceuticals, Inc. 7 BLISTER PACK in 1 PACKAGE, COMBINATION (69102-300-01) / 1 KIT in 1 BLISTER PACK
69102-319-01 69102-319 HUMAN PRESCRIPTION DRUG SUBVENITE LAMOTRIGINE TABLET ORAL 20180310 N/A ANDA ANDA078947 OWP Pharmaceuticals, Inc. LAMOTRIGINE 100 mg/1 100 TABLET in 1 BOTTLE (69102-319-01)
69102-319-02 69102-319 HUMAN PRESCRIPTION DRUG SUBVENITE LAMOTRIGINE TABLET ORAL 20180310 N/A ANDA ANDA078947 OWP Pharmaceuticals, Inc. LAMOTRIGINE 100 mg/1 2500 TABLET in 1 BOTTLE (69102-319-02)
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