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=ANDA201779"
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
68001-249-01 68001-249 HUMAN PRESCRIPTION DRUG Zolmitriptan Zolmitriptan TABLET, FILM COATED ORAL 20140313 N/A ANDA ANDA201779 BluePoint Laboratories ZOLMITRIPTAN 2.5 mg/1 1 BLISTER PACK in 1 CARTON (68001-249-01) / 6 TABLET, FILM COATED in 1 BLISTER PACK (68001-249-19)
68001-250-01 68001-250 HUMAN PRESCRIPTION DRUG Zolmitriptan Zolmitriptan TABLET, FILM COATED ORAL 20140313 N/A ANDA ANDA201779 BluePoint Laboratories ZOLMITRIPTAN 5 mg/1 1 BLISTER PACK in 1 CARTON (68001-250-01) / 3 TABLET, FILM COATED in 1 BLISTER PACK (68001-250-18)
68462-497-76 68462-497 HUMAN PRESCRIPTION DRUG Zolmitriptan Zolmitriptan TABLET, FILM COATED ORAL 20130514 N/A ANDA ANDA201779 Glenmark Pharmaceuticals Inc.,USA ZOLMITRIPTAN 2.5 mg/1 1 BLISTER PACK in 1 CARTON (68462-497-76) / 6 TABLET, FILM COATED in 1 BLISTER PACK
68462-498-33 68462-498 HUMAN PRESCRIPTION DRUG Zolmitriptan Zolmitriptan TABLET, FILM COATED ORAL 20130514 N/A ANDA ANDA201779 Glenmark Pharmaceuticals Inc.,USA ZOLMITRIPTAN 5 mg/1 1 BLISTER PACK in 1 CARTON (68462-498-33) / 3 TABLET, FILM COATED in 1 BLISTER PACK
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