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=ANDA040604"
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
0904-6618-61 0904-6618 HUMAN PRESCRIPTION DRUG Hydroxyzine Hydrochloride Hydroxyzine Hydrochloride TABLET, FILM COATED ORAL 20150331 N/A ANDA ANDA040604 Major Pharmaceuticals HYDROXYZINE DIHYDROCHLORIDE 50 mg/1 100 BLISTER PACK in 1 CARTON (0904-6618-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK
42806-161-01 42806-161 HUMAN PRESCRIPTION DRUG Hydroxyzine Hydrochloride Hydroxyzine Hydrochloride TABLET, FILM COATED ORAL 20150331 N/A ANDA ANDA040604 Epic Pharma, LLC HYDROXYZINE DIHYDROCHLORIDE 50 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (42806-161-01)
42806-161-05 42806-161 HUMAN PRESCRIPTION DRUG Hydroxyzine Hydrochloride Hydroxyzine Hydrochloride TABLET, FILM COATED ORAL 20150331 N/A ANDA ANDA040604 Epic Pharma, LLC HYDROXYZINE DIHYDROCHLORIDE 50 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (42806-161-05)
42806-161-10 42806-161 HUMAN PRESCRIPTION DRUG Hydroxyzine Hydrochloride Hydroxyzine Hydrochloride TABLET, FILM COATED ORAL 20150331 N/A ANDA ANDA040604 Epic Pharma, LLC HYDROXYZINE DIHYDROCHLORIDE 50 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (42806-161-10)
72162-2167-0 72162-2167 HUMAN PRESCRIPTION DRUG Hydroxyzine Hydrochloride Hydroxyzine Hydrochloride TABLET, FILM COATED ORAL 20231207 N/A ANDA ANDA040604 Bryant Ranch Prepack HYDROXYZINE DIHYDROCHLORIDE 50 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (72162-2167-0)
55154-7994-0 55154-7994 HUMAN PRESCRIPTION DRUG Hydroxyzine Hydrochloride Hydroxyzine Hydrochloride TABLET, FILM COATED ORAL 20150331 N/A ANDA ANDA040604 Cardinal Health 107, LLC HYDROXYZINE DIHYDROCHLORIDE 25 mg/1 10 BLISTER PACK in 1 BAG (55154-7994-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK
71205-332-15 71205-332 HUMAN PRESCRIPTION DRUG Hydroxyzine Hydrochloride Hydroxyzine Hydrochloride TABLET, FILM COATED ORAL 20190901 N/A ANDA ANDA040604 Proficient Rx LP HYDROXYZINE DIHYDROCHLORIDE 50 mg/1 15 TABLET, FILM COATED in 1 BOTTLE (71205-332-15)
71205-332-20 71205-332 HUMAN PRESCRIPTION DRUG Hydroxyzine Hydrochloride Hydroxyzine Hydrochloride TABLET, FILM COATED ORAL 20190901 N/A ANDA ANDA040604 Proficient Rx LP HYDROXYZINE DIHYDROCHLORIDE 50 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (71205-332-20)
71205-332-30 71205-332 HUMAN PRESCRIPTION DRUG Hydroxyzine Hydrochloride Hydroxyzine Hydrochloride TABLET, FILM COATED ORAL 20190901 N/A ANDA ANDA040604 Proficient Rx LP HYDROXYZINE DIHYDROCHLORIDE 50 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71205-332-30)
71205-332-60 71205-332 HUMAN PRESCRIPTION DRUG Hydroxyzine Hydrochloride Hydroxyzine Hydrochloride TABLET, FILM COATED ORAL 20190901 N/A ANDA ANDA040604 Proficient Rx LP HYDROXYZINE DIHYDROCHLORIDE 50 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71205-332-60)
71205-332-90 71205-332 HUMAN PRESCRIPTION DRUG Hydroxyzine Hydrochloride Hydroxyzine Hydrochloride TABLET, FILM COATED ORAL 20190901 N/A ANDA ANDA040604 Proficient Rx LP HYDROXYZINE DIHYDROCHLORIDE 50 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71205-332-90)
67046-1296-3 67046-1296 HUMAN PRESCRIPTION DRUG Hydroxyzine Hydrochloride Hydroxyzine Hydrochloride TABLET, FILM COATED ORAL 20241113 N/A ANDA ANDA040604 Coupler LLC HYDROXYZINE DIHYDROCHLORIDE 50 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1296-3)
71335-2185-1 71335-2185 HUMAN PRESCRIPTION DRUG Hydroxyzine Hydrochloride Hydroxyzine Hydrochloride TABLET, FILM COATED ORAL 20240403 N/A ANDA ANDA040604 Bryant Ranch Prepack HYDROXYZINE DIHYDROCHLORIDE 50 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (71335-2185-1)
71335-2185-2 71335-2185 HUMAN PRESCRIPTION DRUG Hydroxyzine Hydrochloride Hydroxyzine Hydrochloride TABLET, FILM COATED ORAL 20240403 N/A ANDA ANDA040604 Bryant Ranch Prepack HYDROXYZINE DIHYDROCHLORIDE 50 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (71335-2185-2)
71335-2185-3 71335-2185 HUMAN PRESCRIPTION DRUG Hydroxyzine Hydrochloride Hydroxyzine Hydrochloride TABLET, FILM COATED ORAL 20230124 N/A ANDA ANDA040604 Bryant Ranch Prepack HYDROXYZINE DIHYDROCHLORIDE 50 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71335-2185-3)
71335-2185-4 71335-2185 HUMAN PRESCRIPTION DRUG Hydroxyzine Hydrochloride Hydroxyzine Hydrochloride TABLET, FILM COATED ORAL 20221129 N/A ANDA ANDA040604 Bryant Ranch Prepack HYDROXYZINE DIHYDROCHLORIDE 50 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71335-2185-4)
71335-2185-5 71335-2185 HUMAN PRESCRIPTION DRUG Hydroxyzine Hydrochloride Hydroxyzine Hydrochloride TABLET, FILM COATED ORAL 20240403 N/A ANDA ANDA040604 Bryant Ranch Prepack HYDROXYZINE DIHYDROCHLORIDE 50 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71335-2185-5)
0904-6617-61 0904-6617 HUMAN PRESCRIPTION DRUG Hydroxyzine Hydrochloride Hydroxyzine Hydrochloride TABLET, FILM COATED ORAL 20150331 N/A ANDA ANDA040604 Major Pharmaceuticals HYDROXYZINE DIHYDROCHLORIDE 25 mg/1 100 BLISTER PACK in 1 CARTON (0904-6617-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK
68071-5133-3 68071-5133 HUMAN PRESCRIPTION DRUG Hydroxyzine Hydrochloride Hydroxyzine Hydrochloride TABLET, FILM COATED ORAL 20241015 N/A ANDA ANDA040604 NuCare Pharmaceuticals,Inc. HYDROXYZINE DIHYDROCHLORIDE 50 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68071-5133-3)
68071-5133-6 68071-5133 HUMAN PRESCRIPTION DRUG Hydroxyzine Hydrochloride Hydroxyzine Hydrochloride TABLET, FILM COATED ORAL 20191213 N/A ANDA ANDA040604 NuCare Pharmaceuticals,Inc. HYDROXYZINE DIHYDROCHLORIDE 50 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (68071-5133-6)
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