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=ANDA203019"
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
65841-765-86 65841-765 HUMAN PRESCRIPTION DRUG Zolmitriptan Zolmitriptan TABLET, FILM COATED ORAL 20181112 N/A ANDA ANDA203019 Zydus Lifesciences Limited ZOLMITRIPTAN 2.5 mg/1 1 BLISTER PACK in 1 CARTON (65841-765-86) / 6 TABLET, FILM COATED in 1 BLISTER PACK
65841-766-82 65841-766 HUMAN PRESCRIPTION DRUG Zolmitriptan Zolmitriptan TABLET, FILM COATED ORAL 20181112 N/A ANDA ANDA203019 Zydus Lifesciences Limited ZOLMITRIPTAN 5 mg/1 1 BLISTER PACK in 1 CARTON (65841-766-82) / 3 TABLET, FILM COATED in 1 BLISTER PACK
68382-714-82 68382-714 HUMAN PRESCRIPTION DRUG Zolmitriptan Zolmitriptan TABLET, FILM COATED ORAL 20181112 N/A ANDA ANDA203019 Zydus Pharmaceuticals USA Inc. ZOLMITRIPTAN 5 mg/1 1 BLISTER PACK in 1 CARTON (68382-714-82) / 3 TABLET, FILM COATED in 1 BLISTER PACK (68382-714-87)
68382-712-86 68382-712 HUMAN PRESCRIPTION DRUG Zolmitriptan Zolmitriptan TABLET, FILM COATED ORAL 20181112 N/A ANDA ANDA203019 Zydus Pharmaceuticals USA Inc. ZOLMITRIPTAN 2.5 mg/1 1 BLISTER PACK in 1 CARTON (68382-712-86) / 6 TABLET, FILM COATED in 1 BLISTER PACK (68382-712-69)
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