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=ANDA090191"
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
61037-479-02 61037-479 HUMAN PRESCRIPTION DRUG CETIRIZINE HYDROCHLORIDE CETIRIZINE HYDROCHLORIDE SOLUTION ORAL 20230912 N/A ANDA ANDA090191 BAJAJ MEDICAL, LLC CETIRIZINE HYDROCHLORIDE 1 mg/mL 120 mL in 1 BOTTLE, PLASTIC (61037-479-02)
61037-479-03 61037-479 HUMAN PRESCRIPTION DRUG CETIRIZINE HYDROCHLORIDE CETIRIZINE HYDROCHLORIDE SOLUTION ORAL 20240716 N/A ANDA ANDA090191 BAJAJ MEDICAL, LLC CETIRIZINE HYDROCHLORIDE 1 mg/mL 480 mL in 1 BOTTLE, PLASTIC (61037-479-03)
16571-134-12 16571-134 HUMAN PRESCRIPTION DRUG CETIRIZINE HYDROCHLORIDE CETIRIZINE HYDROCHLORIDE SOLUTION ORAL 20240716 N/A ANDA ANDA090191 Rising Pharma Holdings, Inc. CETIRIZINE HYDROCHLORIDE 1 mg/mL 120 mL in 1 BOTTLE, PLASTIC (16571-134-12)
16571-134-48 16571-134 HUMAN PRESCRIPTION DRUG CETIRIZINE HYDROCHLORIDE CETIRIZINE HYDROCHLORIDE SOLUTION ORAL 20240716 N/A ANDA ANDA090191 Rising Pharma Holdings, Inc. CETIRIZINE HYDROCHLORIDE 1 mg/mL 480 mL in 1 BOTTLE, PLASTIC (16571-134-48)
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