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=ANDA204232"
符合检索条件的记录共 4 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
62332-463-03 62332-463 HUMAN PRESCRIPTION DRUG Zolmitriptan Zolmitriptan TABLET, FILM COATED ORAL 20240110 N/A ANDA ANDA204232 Alembic Pharmaceuticals Inc. ZOLMITRIPTAN 5 mg/1 3 TABLET, FILM COATED in 1 CARTON (62332-463-03)
62332-462-06 62332-462 HUMAN PRESCRIPTION DRUG Zolmitriptan Zolmitriptan TABLET, FILM COATED ORAL 20240110 N/A ANDA ANDA204232 Alembic Pharmaceuticals Inc. ZOLMITRIPTAN 2.5 mg/1 6 TABLET, FILM COATED in 1 CARTON (62332-462-06)
46708-463-03 46708-463 HUMAN PRESCRIPTION DRUG Zolmitriptan Zolmitriptan TABLET, FILM COATED ORAL 20160104 N/A ANDA ANDA204232 Alembic Pharmaceuticals Limited ZOLMITRIPTAN 5 mg/1 3 TABLET, FILM COATED in 1 CARTON (46708-463-03)
46708-462-06 46708-462 HUMAN PRESCRIPTION DRUG Zolmitriptan Zolmitriptan TABLET, FILM COATED ORAL 20160104 N/A ANDA ANDA204232 Alembic Pharmaceuticals Limited ZOLMITRIPTAN 2.5 mg/1 6 TABLET, FILM COATED in 1 CARTON (46708-462-06)
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