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"
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
72189-577-60 72189-577 HUMAN PRESCRIPTION DRUG Hydroxyzine HCL Hydroxyzine HCL TABLET, FILM COATED ORAL 20240913 N/A ANDA ANDA217652 Direct_rx HYDROXYZINE DIHYDROCHLORIDE 50 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (72189-577-60)
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)
69844-071-01 69844-071 HUMAN PRESCRIPTION DRUG HYDROXYZINE HYDROCHLORIDE hydroxyzine hydrochloride TABLET, FILM COATED ORAL 20230822 N/A ANDA ANDA217652 Graviti Pharmaceuticals Private Limited HYDROXYZINE DIHYDROCHLORIDE 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (69844-071-01)
69844-071-02 69844-071 HUMAN PRESCRIPTION DRUG HYDROXYZINE HYDROCHLORIDE hydroxyzine hydrochloride TABLET, FILM COATED ORAL 20230822 N/A ANDA ANDA217652 Graviti Pharmaceuticals Private Limited HYDROXYZINE DIHYDROCHLORIDE 10 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (69844-071-02)
69844-071-03 69844-071 HUMAN PRESCRIPTION DRUG HYDROXYZINE HYDROCHLORIDE hydroxyzine hydrochloride TABLET, FILM COATED ORAL 20230822 N/A ANDA ANDA217652 Graviti Pharmaceuticals Private Limited HYDROXYZINE DIHYDROCHLORIDE 10 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (69844-071-03)
69844-072-01 69844-072 HUMAN PRESCRIPTION DRUG HYDROXYZINE HYDROCHLORIDE hydroxyzine hydrochloride TABLET, FILM COATED ORAL 20230822 N/A ANDA ANDA217652 Graviti Pharmaceuticals Private Limited HYDROXYZINE DIHYDROCHLORIDE 25 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (69844-072-01)
69844-072-02 69844-072 HUMAN PRESCRIPTION DRUG HYDROXYZINE HYDROCHLORIDE hydroxyzine hydrochloride TABLET, FILM COATED ORAL 20230822 N/A ANDA ANDA217652 Graviti Pharmaceuticals Private Limited HYDROXYZINE DIHYDROCHLORIDE 25 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (69844-072-02)
69844-072-03 69844-072 HUMAN PRESCRIPTION DRUG HYDROXYZINE HYDROCHLORIDE hydroxyzine hydrochloride TABLET, FILM COATED ORAL 20230822 N/A ANDA ANDA217652 Graviti Pharmaceuticals Private Limited HYDROXYZINE DIHYDROCHLORIDE 25 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (69844-072-03)
69844-073-01 69844-073 HUMAN PRESCRIPTION DRUG HYDROXYZINE HYDROCHLORIDE hydroxyzine hydrochloride TABLET, FILM COATED ORAL 20230822 N/A ANDA ANDA217652 Graviti Pharmaceuticals Private Limited HYDROXYZINE DIHYDROCHLORIDE 50 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (69844-073-01)
69844-073-02 69844-073 HUMAN PRESCRIPTION DRUG HYDROXYZINE HYDROCHLORIDE hydroxyzine hydrochloride TABLET, FILM COATED ORAL 20230822 N/A ANDA ANDA217652 Graviti Pharmaceuticals Private Limited HYDROXYZINE DIHYDROCHLORIDE 50 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (69844-073-02)
69844-073-03 69844-073 HUMAN PRESCRIPTION DRUG HYDROXYZINE HYDROCHLORIDE hydroxyzine hydrochloride TABLET, FILM COATED ORAL 20230822 N/A ANDA ANDA217652 Graviti Pharmaceuticals Private Limited HYDROXYZINE DIHYDROCHLORIDE 50 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (69844-073-03)
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)
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)
50090-7327-0 50090-7327 HUMAN PRESCRIPTION DRUG HYDROXYZINE HYDROCHLORIDE hydroxyzine hydrochloride TABLET, FILM COATED ORAL 20241015 N/A ANDA ANDA217652 A-S Medication Solutions HYDROXYZINE DIHYDROCHLORIDE 25 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (50090-7327-0)
50090-7330-0 50090-7330 HUMAN PRESCRIPTION DRUG HYDROXYZINE HYDROCHLORIDE hydroxyzine hydrochloride TABLET, FILM COATED ORAL 20241015 N/A ANDA ANDA217652 A-S Medication Solutions HYDROXYZINE DIHYDROCHLORIDE 25 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (50090-7330-0)
50090-7330-1 50090-7330 HUMAN PRESCRIPTION DRUG HYDROXYZINE HYDROCHLORIDE hydroxyzine hydrochloride TABLET, FILM COATED ORAL 20241015 N/A ANDA ANDA217652 A-S Medication Solutions HYDROXYZINE DIHYDROCHLORIDE 25 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (50090-7330-1)
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