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=ANDA202890"
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
68382-715-86 68382-715 HUMAN PRESCRIPTION DRUG Zolmitriptan Zolmitriptan TABLET, ORALLY DISINTEGRATING ORAL 20130516 N/A ANDA ANDA202890 Zydus Pharmaceuticals USA Inc. ZOLMITRIPTAN 2.5 mg/1 1 BLISTER PACK in 1 CARTON (68382-715-86) / 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (68382-715-69)
68382-717-10 68382-717 HUMAN PRESCRIPTION DRUG Zolmitriptan Zolmitriptan TABLET, ORALLY DISINTEGRATING ORAL 20130516 N/A ANDA ANDA202890 Zydus Pharmaceuticals USA Inc. ZOLMITRIPTAN 5 mg/1 1000 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (68382-717-10)
68382-717-16 68382-717 HUMAN PRESCRIPTION DRUG Zolmitriptan Zolmitriptan TABLET, ORALLY DISINTEGRATING ORAL 20130516 N/A ANDA ANDA202890 Zydus Pharmaceuticals USA Inc. ZOLMITRIPTAN 5 mg/1 90 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (68382-717-16)
68382-715-01 68382-715 HUMAN PRESCRIPTION DRUG Zolmitriptan Zolmitriptan TABLET, ORALLY DISINTEGRATING ORAL 20130516 N/A ANDA ANDA202890 Zydus Pharmaceuticals USA Inc. ZOLMITRIPTAN 2.5 mg/1 100 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (68382-715-01)
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