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=NDA022497"
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
24979-248-06 24979-248 HUMAN PRESCRIPTION DRUG bupropion hydrochloride bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20231215 N/A NDA AUTHORIZED GENERIC NDA022497 Upsher-Smith Laboratories, LLC BUPROPION HYDROCHLORIDE 450 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (24979-248-06)
24979-247-06 24979-247 HUMAN PRESCRIPTION DRUG Forfivo XL bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20231215 N/A NDA NDA022497 Upsher-Smith Laboratories, LLC BUPROPION HYDROCHLORIDE 450 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (24979-247-06)
47781-637-30 47781-637 HUMAN PRESCRIPTION DRUG bupropion hydrochloride bupropion hydrochloride TABLET, FILM COATED, EXTENDED RELEASE ORAL 20180928 20260301 NDA AUTHORIZED GENERIC NDA022497 Alvogen Inc. BUPROPION HYDROCHLORIDE 450 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47781-637-30)
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