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=ANDA207867"
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
63548-0102-3 63548-0102 HUMAN PRESCRIPTION DRUG Zolmitriptan Zolmitriptan TABLET, FILM COATED ORAL 20170227 N/A ANDA ANDA207867 PLD Acquisitions LLC DBA Avéma Pharma Solutions ZOLMITRIPTAN 5 mg/1 1 BLISTER PACK in 1 CARTON (63548-0102-3) / 3 TABLET, FILM COATED in 1 BLISTER PACK
63548-0101-6 63548-0101 HUMAN PRESCRIPTION DRUG Zolmitriptan Zolmitriptan TABLET, FILM COATED ORAL 20170227 N/A ANDA ANDA207867 PLD Acquisitions LLC DBA Avéma Pharma Solutions ZOLMITRIPTAN 2.5 mg/1 1 BLISTER PACK in 1 CARTON (63548-0101-6) / 6 TABLET, FILM COATED in 1 BLISTER PACK
60846-133-60 60846-133 HUMAN PRESCRIPTION DRUG ZOMIG zolmitriptan TABLET, FILM COATED ORAL 20230109 N/A ANDA ANDA207867 Amneal Pharmaceuticals LLC ZOLMITRIPTAN 5 mg/1 1 BLISTER PACK in 1 CARTON (60846-133-60) / 3 TABLET, FILM COATED in 1 BLISTER PACK
60846-130-30 60846-130 HUMAN PRESCRIPTION DRUG ZOMIG zolmitriptan TABLET, FILM COATED ORAL 20230109 N/A ANDA ANDA207867 Amneal Pharmaceuticals LLC ZOLMITRIPTAN 2.5 mg/1 1 BLISTER PACK in 1 CARTON (60846-130-30) / 6 TABLET, FILM COATED in 1 BLISTER PACK
71626-101-06 71626-101 HUMAN PRESCRIPTION DRUG Zolmitriptan Zolmitriptan TABLET, FILM COATED ORAL 20180530 N/A ANDA ANDA207867 Medstone Pharma LLC ZOLMITRIPTAN 2.5 mg/1 6 BLISTER PACK in 1 CARTON (71626-101-06) / 1 TABLET, FILM COATED in 1 BLISTER PACK
71626-102-03 71626-102 HUMAN PRESCRIPTION DRUG Zolmitriptan Zolmitriptan TABLET, FILM COATED ORAL 20180530 N/A ANDA ANDA207867 Medstone Pharma LLC ZOLMITRIPTAN 5 mg/1 3 BLISTER PACK in 1 CARTON (71626-102-03) / 1 TABLET, FILM COATED in 1 BLISTER PACK
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