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=ANDA217652"
符合检索条件的记录共 45 条，共 3 页，当前第 2 页 ，可点击列名称排序
首页 上一页 下一页 最后一页
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
60760-990-30 60760-990 HUMAN PRESCRIPTION DRUG HYDROXYZINE HYDROCHLORIDE hydroxyzine hydrochloride TABLET, FILM COATED ORAL 20250319 N/A ANDA ANDA217652 ST. MARY'S MEDICAL PARK PHARMACY HYDROXYZINE DIHYDROCHLORIDE 25 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-990-30)
70518-4141-0 70518-4141 HUMAN PRESCRIPTION DRUG HYDROXYZINE HYDROCHLORIDE hydroxyzine hydrochloride TABLET, FILM COATED ORAL 20240716 N/A ANDA ANDA217652 REMEDYREPACK INC. HYDROXYZINE DIHYDROCHLORIDE 25 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4141-0)
70518-4141-1 70518-4141 HUMAN PRESCRIPTION DRUG HYDROXYZINE HYDROCHLORIDE hydroxyzine hydrochloride TABLET, FILM COATED ORAL 20250326 N/A ANDA ANDA217652 REMEDYREPACK INC. HYDROXYZINE DIHYDROCHLORIDE 25 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4141-1)
70518-4141-2 70518-4141 HUMAN PRESCRIPTION DRUG HYDROXYZINE HYDROCHLORIDE hydroxyzine hydrochloride TABLET, FILM COATED ORAL 20250715 N/A ANDA ANDA217652 REMEDYREPACK INC. HYDROXYZINE DIHYDROCHLORIDE 25 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4141-2)
70518-4170-0 70518-4170 HUMAN PRESCRIPTION DRUG HYDROXYZINE HYDROCHLORIDE hydroxyzine hydrochloride TABLET, FILM COATED ORAL 20240828 N/A ANDA ANDA217652 REMEDYREPACK INC. HYDROXYZINE DIHYDROCHLORIDE 50 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4170-0)
70518-4170-1 70518-4170 HUMAN PRESCRIPTION DRUG HYDROXYZINE HYDROCHLORIDE hydroxyzine hydrochloride TABLET, FILM COATED ORAL 20250404 N/A ANDA ANDA217652 REMEDYREPACK INC. HYDROXYZINE DIHYDROCHLORIDE 50 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4170-1)
70518-4170-2 70518-4170 HUMAN PRESCRIPTION DRUG HYDROXYZINE HYDROCHLORIDE hydroxyzine hydrochloride TABLET, FILM COATED ORAL 20250708 N/A ANDA ANDA217652 REMEDYREPACK INC. HYDROXYZINE DIHYDROCHLORIDE 50 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4170-2)
70518-4170-3 70518-4170 HUMAN PRESCRIPTION DRUG HYDROXYZINE HYDROCHLORIDE hydroxyzine hydrochloride TABLET, FILM COATED ORAL 20251024 N/A ANDA ANDA217652 REMEDYREPACK INC. HYDROXYZINE DIHYDROCHLORIDE 50 mg/1 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4170-3)
68788-8707-3 68788-8707 HUMAN PRESCRIPTION DRUG HYDROXYZINE HYDROCHLORIDE hydroxyzine hydrochloride TABLET, FILM COATED ORAL 20240701 N/A ANDA ANDA217652 Preferred Pharmaceuticals Inc. HYDROXYZINE DIHYDROCHLORIDE 25 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68788-8707-3)
68788-8707-6 68788-8707 HUMAN PRESCRIPTION DRUG HYDROXYZINE HYDROCHLORIDE hydroxyzine hydrochloride TABLET, FILM COATED ORAL 20240701 N/A ANDA ANDA217652 Preferred Pharmaceuticals Inc. HYDROXYZINE DIHYDROCHLORIDE 25 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (68788-8707-6)
68788-8707-9 68788-8707 HUMAN PRESCRIPTION DRUG HYDROXYZINE HYDROCHLORIDE hydroxyzine hydrochloride TABLET, FILM COATED ORAL 20240701 N/A ANDA ANDA217652 Preferred Pharmaceuticals Inc. HYDROXYZINE DIHYDROCHLORIDE 25 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68788-8707-9)
71335-2410-1 71335-2410 HUMAN PRESCRIPTION DRUG HYDROXYZINE HYDROCHLORIDE hydroxyzine hydrochloride TABLET, FILM COATED ORAL 20240610 N/A ANDA ANDA217652 Bryant Ranch Prepack HYDROXYZINE DIHYDROCHLORIDE 50 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (71335-2410-1)
71335-2410-2 71335-2410 HUMAN PRESCRIPTION DRUG HYDROXYZINE HYDROCHLORIDE hydroxyzine hydrochloride TABLET, FILM COATED ORAL 20240610 N/A ANDA ANDA217652 Bryant Ranch Prepack HYDROXYZINE DIHYDROCHLORIDE 50 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (71335-2410-2)
71335-2410-3 71335-2410 HUMAN PRESCRIPTION DRUG HYDROXYZINE HYDROCHLORIDE hydroxyzine hydrochloride TABLET, FILM COATED ORAL 20240610 N/A ANDA ANDA217652 Bryant Ranch Prepack HYDROXYZINE DIHYDROCHLORIDE 50 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71335-2410-3)
71335-2410-4 71335-2410 HUMAN PRESCRIPTION DRUG HYDROXYZINE HYDROCHLORIDE hydroxyzine hydrochloride TABLET, FILM COATED ORAL 20240610 N/A ANDA ANDA217652 Bryant Ranch Prepack HYDROXYZINE DIHYDROCHLORIDE 50 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71335-2410-4)
71335-2410-5 71335-2410 HUMAN PRESCRIPTION DRUG HYDROXYZINE HYDROCHLORIDE hydroxyzine hydrochloride TABLET, FILM COATED ORAL 20240610 N/A ANDA ANDA217652 Bryant Ranch Prepack HYDROXYZINE DIHYDROCHLORIDE 50 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71335-2410-5)
68788-8872-3 68788-8872 HUMAN PRESCRIPTION DRUG HYDROXYZINE HYDROCHLORIDE hydroxyzine hydrochloride TABLET, FILM COATED ORAL 20250501 N/A ANDA ANDA217652 Preferred Pharmaceuticals Inc. HYDROXYZINE DIHYDROCHLORIDE 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68788-8872-3)
71335-2636-1 71335-2636 HUMAN PRESCRIPTION DRUG HYDROXYZINE HYDROCHLORIDE hydroxyzine hydrochloride TABLET, FILM COATED ORAL 20250602 N/A ANDA ANDA217652 Bryant Ranch Prepack HYDROXYZINE HYDROCHLORIDE 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71335-2636-1)
71335-2636-2 71335-2636 HUMAN PRESCRIPTION DRUG HYDROXYZINE HYDROCHLORIDE hydroxyzine hydrochloride TABLET, FILM COATED ORAL 20250602 N/A ANDA ANDA217652 Bryant Ranch Prepack HYDROXYZINE HYDROCHLORIDE 10 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (71335-2636-2)
71335-2636-3 71335-2636 HUMAN PRESCRIPTION DRUG HYDROXYZINE HYDROCHLORIDE hydroxyzine hydrochloride TABLET, FILM COATED ORAL 20250602 N/A ANDA ANDA217652 Bryant Ranch Prepack HYDROXYZINE HYDROCHLORIDE 10 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (71335-2636-3)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2025 Drugfuture->U.S. FDA National Drug Code DataBase