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=ANDA087871"
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
72162-2512-0 72162-2512 HUMAN PRESCRIPTION DRUG Hydroxyzine Hydrochloride Hydroxyzine Hydrochloride TABLET, FILM COATED ORAL 20250523 N/A ANDA ANDA087871 Bryant Ranch Prepack HYDROXYZINE DIHYDROCHLORIDE 25 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (72162-2512-0)
72162-2512-1 72162-2512 HUMAN PRESCRIPTION DRUG Hydroxyzine Hydrochloride Hydroxyzine Hydrochloride TABLET, FILM COATED ORAL 20250523 N/A ANDA ANDA087871 Bryant Ranch Prepack HYDROXYZINE DIHYDROCHLORIDE 25 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (72162-2512-1)
72162-2512-5 72162-2512 HUMAN PRESCRIPTION DRUG Hydroxyzine Hydrochloride Hydroxyzine Hydrochloride TABLET, FILM COATED ORAL 20250523 N/A ANDA ANDA087871 Bryant Ranch Prepack HYDROXYZINE DIHYDROCHLORIDE 25 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (72162-2512-5)
71335-3035-1 71335-3035 HUMAN PRESCRIPTION DRUG Hydroxyzine Hydrochloride Hydroxyzine Hydrochloride TABLET, FILM COATED ORAL 20251203 N/A ANDA ANDA087871 Bryant Ranch Prepack HYDROXYZINE DIHYDROCHLORIDE 25 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (71335-3035-1)
59651-501-01 59651-501 HUMAN PRESCRIPTION DRUG Hydroxyzine Hydrochloride Hydroxyzine Hydrochloride TABLET, FILM COATED ORAL 20211007 N/A ANDA ANDA087871 Aurobindo Pharma Limited HYDROXYZINE DIHYDROCHLORIDE 50 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (59651-501-01)
59651-501-05 59651-501 HUMAN PRESCRIPTION DRUG Hydroxyzine Hydrochloride Hydroxyzine Hydrochloride TABLET, FILM COATED ORAL 20211007 N/A ANDA ANDA087871 Aurobindo Pharma Limited HYDROXYZINE DIHYDROCHLORIDE 50 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (59651-501-05)
59651-501-99 59651-501 HUMAN PRESCRIPTION DRUG Hydroxyzine Hydrochloride Hydroxyzine Hydrochloride TABLET, FILM COATED ORAL 20211007 N/A ANDA ANDA087871 Aurobindo Pharma Limited HYDROXYZINE DIHYDROCHLORIDE 50 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (59651-501-99)
72162-2513-0 72162-2513 HUMAN PRESCRIPTION DRUG Hydroxyzine Hydrochloride Hydroxyzine Hydrochloride TABLET, FILM COATED ORAL 20250523 N/A ANDA ANDA087871 Bryant Ranch Prepack HYDROXYZINE DIHYDROCHLORIDE 50 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (72162-2513-0)
72162-2513-1 72162-2513 HUMAN PRESCRIPTION DRUG Hydroxyzine Hydrochloride Hydroxyzine Hydrochloride TABLET, FILM COATED ORAL 20250523 N/A ANDA ANDA087871 Bryant Ranch Prepack HYDROXYZINE DIHYDROCHLORIDE 50 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (72162-2513-1)
72162-2513-5 72162-2513 HUMAN PRESCRIPTION DRUG Hydroxyzine Hydrochloride Hydroxyzine Hydrochloride TABLET, FILM COATED ORAL 20250523 N/A ANDA ANDA087871 Bryant Ranch Prepack HYDROXYZINE DIHYDROCHLORIDE 50 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (72162-2513-5)
71335-3088-1 71335-3088 HUMAN PRESCRIPTION DRUG Hydroxyzine Hydrochloride Hydroxyzine Hydrochloride TABLET, FILM COATED ORAL 20260217 N/A ANDA ANDA087871 Bryant Ranch Prepack HYDROXYZINE DIHYDROCHLORIDE 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71335-3088-1)
71335-3088-2 71335-3088 HUMAN PRESCRIPTION DRUG Hydroxyzine Hydrochloride Hydroxyzine Hydrochloride TABLET, FILM COATED ORAL 20260217 N/A ANDA ANDA087871 Bryant Ranch Prepack HYDROXYZINE DIHYDROCHLORIDE 10 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (71335-3088-2)
71335-3088-3 71335-3088 HUMAN PRESCRIPTION DRUG Hydroxyzine Hydrochloride Hydroxyzine Hydrochloride TABLET, FILM COATED ORAL 20260217 N/A ANDA ANDA087871 Bryant Ranch Prepack HYDROXYZINE DIHYDROCHLORIDE 10 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (71335-3088-3)
71335-3088-4 71335-3088 HUMAN PRESCRIPTION DRUG Hydroxyzine Hydrochloride Hydroxyzine Hydrochloride TABLET, FILM COATED ORAL 20260217 N/A ANDA ANDA087871 Bryant Ranch Prepack HYDROXYZINE DIHYDROCHLORIDE 10 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71335-3088-4)
71335-3088-5 71335-3088 HUMAN PRESCRIPTION DRUG Hydroxyzine Hydrochloride Hydroxyzine Hydrochloride TABLET, FILM COATED ORAL 20260217 N/A ANDA ANDA087871 Bryant Ranch Prepack HYDROXYZINE DIHYDROCHLORIDE 10 mg/1 15 TABLET, FILM COATED in 1 BOTTLE (71335-3088-5)
71335-3088-6 71335-3088 HUMAN PRESCRIPTION DRUG Hydroxyzine Hydrochloride Hydroxyzine Hydrochloride TABLET, FILM COATED ORAL 20260217 N/A ANDA ANDA087871 Bryant Ranch Prepack HYDROXYZINE DIHYDROCHLORIDE 10 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71335-3088-6)
71335-3088-7 71335-3088 HUMAN PRESCRIPTION DRUG Hydroxyzine Hydrochloride Hydroxyzine Hydrochloride TABLET, FILM COATED ORAL 20260217 N/A ANDA ANDA087871 Bryant Ranch Prepack HYDROXYZINE DIHYDROCHLORIDE 10 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (71335-3088-7)
71335-3088-8 71335-3088 HUMAN PRESCRIPTION DRUG Hydroxyzine Hydrochloride Hydroxyzine Hydrochloride TABLET, FILM COATED ORAL 20260217 N/A ANDA ANDA087871 Bryant Ranch Prepack HYDROXYZINE DIHYDROCHLORIDE 10 mg/1 10 TABLET, FILM COATED in 1 BOTTLE (71335-3088-8)
71335-3036-1 71335-3036 HUMAN PRESCRIPTION DRUG Hydroxyzine Hydrochloride Hydroxyzine Hydrochloride TABLET, FILM COATED ORAL 20251203 N/A ANDA ANDA087871 Bryant Ranch Prepack HYDROXYZINE DIHYDROCHLORIDE 50 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (71335-3036-1)
72162-2511-1 72162-2511 HUMAN PRESCRIPTION DRUG Hydroxyzine Hydrochloride Hydroxyzine Hydrochloride TABLET, FILM COATED ORAL 20250523 N/A ANDA ANDA087871 Bryant Ranch Prepack HYDROXYZINE DIHYDROCHLORIDE 10 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (72162-2511-1)
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