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=ANDA218543"
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
69238-2860-1 69238-2860 HUMAN PRESCRIPTION DRUG Mirabegron Mirabegron TABLET, FILM COATED, EXTENDED RELEASE ORAL 20260406 N/A ANDA ANDA218543 Amneal Pharmaceuticals NY LLC MIRABEGRON 25 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (69238-2860-1)
69238-2860-2 69238-2860 HUMAN PRESCRIPTION DRUG Mirabegron Mirabegron TABLET, FILM COATED, EXTENDED RELEASE ORAL 20260406 N/A ANDA ANDA218543 Amneal Pharmaceuticals NY LLC MIRABEGRON 25 mg/1 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (69238-2860-2)
69238-2861-1 69238-2861 HUMAN PRESCRIPTION DRUG Mirabegron Mirabegron TABLET, FILM COATED, EXTENDED RELEASE ORAL 20260406 N/A ANDA ANDA218543 Amneal Pharmaceuticals NY LLC MIRABEGRON 50 mg/1 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (69238-2861-1)
69238-2861-2 69238-2861 HUMAN PRESCRIPTION DRUG Mirabegron Mirabegron TABLET, FILM COATED, EXTENDED RELEASE ORAL 20260406 N/A ANDA ANDA218543 Amneal Pharmaceuticals NY LLC MIRABEGRON 50 mg/1 90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (69238-2861-2)
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