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=ANDA208784"
符合检索条件的记录共 3 条，共 1 页，当前第 1 页 ，可点击列名称排序
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
55154-4848-0 55154-4848 HUMAN PRESCRIPTION DRUG Lansoprazole Lansoprazole TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE ORAL 20180308 N/A ANDA ANDA208784 Cardinal Health 107, LLC LANSOPRAZOLE 30 mg/1 10 BLISTER PACK in 1 BAG (55154-4848-0) / 1 TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE in 1 BLISTER PACK
0093-3009-93 0093-3009 HUMAN PRESCRIPTION DRUG Lansoprazole Lansoprazole TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE ORAL 20180308 N/A ANDA ANDA208784 Teva Pharmaceuticals USA, Inc. LANSOPRAZOLE 30 mg/1 100 BLISTER PACK in 1 CARTON (0093-3009-93) / 1 TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE in 1 BLISTER PACK (0093-3009-19)
0093-3008-93 0093-3008 HUMAN PRESCRIPTION DRUG Lansoprazole Lansoprazole TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE ORAL 20180308 N/A ANDA ANDA208784 Teva Pharmaceuticals USA, Inc. LANSOPRAZOLE 15 mg/1 100 BLISTER PACK in 1 CARTON (0093-3008-93) / 1 TABLET, ORALLY DISINTEGRATING, DELAYED RELEASE in 1 BLISTER PACK (0093-3008-19)
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