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=ANDA213718"
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
27241-207-30 27241-207 HUMAN PRESCRIPTION DRUG Brexpiprazole Brexpiprazole TABLET ORAL 20230203 N/A ANDA ANDA213718 Ajanta Pharma USA Inc. BREXPIPRAZOLE 2 mg/1 30 TABLET in 1 BOTTLE (27241-207-30)
27241-206-30 27241-206 HUMAN PRESCRIPTION DRUG Brexpiprazole Brexpiprazole TABLET ORAL 20230203 N/A ANDA ANDA213718 Ajanta Pharma USA Inc. BREXPIPRAZOLE 1 mg/1 30 TABLET in 1 BOTTLE (27241-206-30)
27241-204-30 27241-204 HUMAN PRESCRIPTION DRUG Brexpiprazole Brexpiprazole TABLET ORAL 20230203 N/A ANDA ANDA213718 Ajanta Pharma USA Inc. BREXPIPRAZOLE .25 mg/1 30 TABLET in 1 BOTTLE (27241-204-30)
27241-208-30 27241-208 HUMAN PRESCRIPTION DRUG Brexpiprazole Brexpiprazole TABLET ORAL 20230203 N/A ANDA ANDA213718 Ajanta Pharma USA Inc. BREXPIPRAZOLE 3 mg/1 30 TABLET in 1 BOTTLE (27241-208-30)
27241-205-30 27241-205 HUMAN PRESCRIPTION DRUG Brexpiprazole Brexpiprazole TABLET ORAL 20230203 N/A ANDA ANDA213718 Ajanta Pharma USA Inc. BREXPIPRAZOLE .5 mg/1 30 TABLET in 1 BOTTLE (27241-205-30)
27241-209-30 27241-209 HUMAN PRESCRIPTION DRUG Brexpiprazole Brexpiprazole TABLET ORAL 20230203 N/A ANDA ANDA213718 Ajanta Pharma USA Inc. BREXPIPRAZOLE 4 mg/1 30 TABLET in 1 BOTTLE (27241-209-30)
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