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=ANDA209488"
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
70771-1752-1 70771-1752 HUMAN PRESCRIPTION DRUG Mirabegron Mirabegron TABLET, EXTENDED RELEASE ORAL 20240123 N/A ANDA ANDA209488 Zydus Lifesciences Limited MIRABEGRON 25 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1752-1)
70771-1752-3 70771-1752 HUMAN PRESCRIPTION DRUG Mirabegron Mirabegron TABLET, EXTENDED RELEASE ORAL 20240123 N/A ANDA ANDA209488 Zydus Lifesciences Limited MIRABEGRON 25 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1752-3)
70771-1752-9 70771-1752 HUMAN PRESCRIPTION DRUG Mirabegron Mirabegron TABLET, EXTENDED RELEASE ORAL 20240123 N/A ANDA ANDA209488 Zydus Lifesciences Limited MIRABEGRON 25 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1752-9)
70771-1753-1 70771-1753 HUMAN PRESCRIPTION DRUG Mirabegron Mirabegron TABLET, EXTENDED RELEASE ORAL 20240123 N/A ANDA ANDA209488 Zydus Lifesciences Limited MIRABEGRON 50 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1753-1)
70771-1753-3 70771-1753 HUMAN PRESCRIPTION DRUG Mirabegron Mirabegron TABLET, EXTENDED RELEASE ORAL 20240123 N/A ANDA ANDA209488 Zydus Lifesciences Limited MIRABEGRON 50 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1753-3)
70771-1753-9 70771-1753 HUMAN PRESCRIPTION DRUG Mirabegron Mirabegron TABLET, EXTENDED RELEASE ORAL 20240123 N/A ANDA ANDA209488 Zydus Lifesciences Limited MIRABEGRON 50 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (70771-1753-9)
70710-1160-1 70710-1160 HUMAN PRESCRIPTION DRUG Mirabegron Mirabegron TABLET, EXTENDED RELEASE ORAL 20240123 N/A ANDA ANDA209488 Zydus Pharmaceuticals (USA) Inc. MIRABEGRON 50 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70710-1160-1)
70710-1160-3 70710-1160 HUMAN PRESCRIPTION DRUG Mirabegron Mirabegron TABLET, EXTENDED RELEASE ORAL 20240123 N/A ANDA ANDA209488 Zydus Pharmaceuticals (USA) Inc. MIRABEGRON 50 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (70710-1160-3)
70710-1160-9 70710-1160 HUMAN PRESCRIPTION DRUG Mirabegron Mirabegron TABLET, EXTENDED RELEASE ORAL 20240123 N/A ANDA ANDA209488 Zydus Pharmaceuticals (USA) Inc. MIRABEGRON 50 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (70710-1160-9)
70710-1159-1 70710-1159 HUMAN PRESCRIPTION DRUG Mirabegron Mirabegron TABLET, EXTENDED RELEASE ORAL 20240123 N/A ANDA ANDA209488 Zydus Pharmaceuticals (USA) Inc. MIRABEGRON 25 mg/1 100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70710-1159-1)
70710-1159-3 70710-1159 HUMAN PRESCRIPTION DRUG Mirabegron Mirabegron TABLET, EXTENDED RELEASE ORAL 20240123 N/A ANDA ANDA209488 Zydus Pharmaceuticals (USA) Inc. MIRABEGRON 25 mg/1 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (70710-1159-3)
70710-1159-9 70710-1159 HUMAN PRESCRIPTION DRUG Mirabegron Mirabegron TABLET, EXTENDED RELEASE ORAL 20240123 N/A ANDA ANDA209488 Zydus Pharmaceuticals (USA) Inc. MIRABEGRON 25 mg/1 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (70710-1159-9)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase