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=ANDA076601"
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
51672-4070-8 51672-4070 HUMAN PRESCRIPTION DRUG Cetirizine Hydrochloride Cetirizine Hydrochloride SOLUTION ORAL 20140501 N/A ANDA ANDA076601 Taro Pharmaceuticals U.S.A., Inc. CETIRIZINE HYDROCHLORIDE 1 mg/mL 1 BOTTLE in 1 CARTON (51672-4070-8) / 120 mL in 1 BOTTLE
71205-435-04 71205-435 HUMAN PRESCRIPTION DRUG Cetirizine Hydrochloride Cetirizine Hydrochloride SOLUTION ORAL 20200319 N/A ANDA ANDA076601 Proficient Rx LP CETIRIZINE HYDROCHLORIDE 1 mg/mL 1 BOTTLE in 1 CARTON (71205-435-04) / 120 mL in 1 BOTTLE
68788-8282-1 68788-8282 HUMAN PRESCRIPTION DRUG Cetirizine Hydrochloride Cetirizine Hydrochloride SOLUTION ORAL 20231025 N/A ANDA ANDA076601 Preferred Pharmaceuticals Inc. CETIRIZINE HYDROCHLORIDE 1 mg/mL 1 BOTTLE in 1 CARTON (68788-8282-1) / 120 mL in 1 BOTTLE
50090-5220-0 50090-5220 HUMAN PRESCRIPTION DRUG Cetirizine Hydrochloride Cetirizine Hydrochloride SOLUTION ORAL 20201007 N/A ANDA ANDA076601 A-S Medication Solutions CETIRIZINE HYDROCHLORIDE 1 mg/mL 1 BOTTLE in 1 CARTON (50090-5220-0) / 120 mL in 1 BOTTLE
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