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=ANDA040659"
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
71335-0153-8 71335-0153 HUMAN PRESCRIPTION DRUG MECLIZINE HYDROCHLORIDE Meclizine Hydrochloride TABLET ORAL 20250911 20261031 ANDA ANDA040659 Bryant Ranch Prepack MECLIZINE HYDROCHLORIDE 12.5 mg/1 10 TABLET in 1 BOTTLE (71335-0153-8)
71335-0153-3 71335-0153 HUMAN PRESCRIPTION DRUG MECLIZINE HYDROCHLORIDE Meclizine Hydrochloride TABLET ORAL 20220223 20261031 ANDA ANDA040659 Bryant Ranch Prepack MECLIZINE HYDROCHLORIDE 12.5 mg/1 90 TABLET in 1 BOTTLE (71335-0153-3)
71335-0153-4 71335-0153 HUMAN PRESCRIPTION DRUG MECLIZINE HYDROCHLORIDE Meclizine Hydrochloride TABLET ORAL 20220223 20261031 ANDA ANDA040659 Bryant Ranch Prepack MECLIZINE HYDROCHLORIDE 12.5 mg/1 28 TABLET in 1 BOTTLE (71335-0153-4)
71335-0153-2 71335-0153 HUMAN PRESCRIPTION DRUG MECLIZINE HYDROCHLORIDE Meclizine Hydrochloride TABLET ORAL 20220223 20261031 ANDA ANDA040659 Bryant Ranch Prepack MECLIZINE HYDROCHLORIDE 12.5 mg/1 60 TABLET in 1 BOTTLE (71335-0153-2)
71335-0503-0 71335-0503 HUMAN PRESCRIPTION DRUG MECLIZINE HYDROCHLORIDE Meclizine Hydrocloride TABLET ORAL 20220223 20261031 ANDA ANDA040659 Bryant Ranch Prepack MECLIZINE HYDROCHLORIDE 25 mg/1 14 TABLET in 1 BOTTLE (71335-0503-0)
71335-0503-4 71335-0503 HUMAN PRESCRIPTION DRUG MECLIZINE HYDROCHLORIDE Meclizine Hydrocloride TABLET ORAL 20220223 20261031 ANDA ANDA040659 Bryant Ranch Prepack MECLIZINE HYDROCHLORIDE 25 mg/1 20 TABLET in 1 BOTTLE (71335-0503-4)
71335-0503-5 71335-0503 HUMAN PRESCRIPTION DRUG MECLIZINE HYDROCHLORIDE Meclizine Hydrocloride TABLET ORAL 20220223 20261031 ANDA ANDA040659 Bryant Ranch Prepack MECLIZINE HYDROCHLORIDE 25 mg/1 40 TABLET in 1 BOTTLE (71335-0503-5)
71335-0503-6 71335-0503 HUMAN PRESCRIPTION DRUG MECLIZINE HYDROCHLORIDE Meclizine Hydrocloride TABLET ORAL 20220223 20261031 ANDA ANDA040659 Bryant Ranch Prepack MECLIZINE HYDROCHLORIDE 25 mg/1 60 TABLET in 1 BOTTLE (71335-0503-6)
71335-0503-7 71335-0503 HUMAN PRESCRIPTION DRUG MECLIZINE HYDROCHLORIDE Meclizine Hydrocloride TABLET ORAL 20220223 20261031 ANDA ANDA040659 Bryant Ranch Prepack MECLIZINE HYDROCHLORIDE 25 mg/1 120 TABLET in 1 BOTTLE (71335-0503-7)
71335-0503-8 71335-0503 HUMAN PRESCRIPTION DRUG MECLIZINE HYDROCHLORIDE Meclizine Hydrocloride TABLET ORAL 20220223 20261031 ANDA ANDA040659 Bryant Ranch Prepack MECLIZINE HYDROCHLORIDE 25 mg/1 10 TABLET in 1 BOTTLE (71335-0503-8)
71335-0503-9 71335-0503 HUMAN PRESCRIPTION DRUG MECLIZINE HYDROCHLORIDE Meclizine Hydrocloride TABLET ORAL 20220223 20261031 ANDA ANDA040659 Bryant Ranch Prepack MECLIZINE HYDROCHLORIDE 25 mg/1 100 TABLET in 1 BOTTLE (71335-0503-9)
71335-0503-1 71335-0503 HUMAN PRESCRIPTION DRUG MECLIZINE HYDROCHLORIDE Meclizine Hydrocloride TABLET ORAL 20220223 20261031 ANDA ANDA040659 Bryant Ranch Prepack MECLIZINE HYDROCHLORIDE 25 mg/1 90 TABLET in 1 BOTTLE (71335-0503-1)
71335-0503-2 71335-0503 HUMAN PRESCRIPTION DRUG MECLIZINE HYDROCHLORIDE Meclizine Hydrocloride TABLET ORAL 20220223 20261031 ANDA ANDA040659 Bryant Ranch Prepack MECLIZINE HYDROCHLORIDE 25 mg/1 30 TABLET in 1 BOTTLE (71335-0503-2)
71335-0503-3 71335-0503 HUMAN PRESCRIPTION DRUG MECLIZINE HYDROCHLORIDE Meclizine Hydrocloride TABLET ORAL 20220223 20261031 ANDA ANDA040659 Bryant Ranch Prepack MECLIZINE HYDROCHLORIDE 25 mg/1 25 TABLET in 1 BOTTLE (71335-0503-3)
70518-1308-0 70518-1308 HUMAN PRESCRIPTION DRUG MECLIZINE HYDROCHLORIDE Meclizine Hydrocloride TABLET ORAL 20180817 20261031 ANDA ANDA040659 REMEDYREPACK INC. MECLIZINE HYDROCHLORIDE 25 mg/1 90 TABLET in 1 BOTTLE, PLASTIC (70518-1308-0)
70518-1308-5 70518-1308 HUMAN PRESCRIPTION DRUG MECLIZINE HYDROCHLORIDE Meclizine Hydrocloride TABLET ORAL 20231218 20261031 ANDA ANDA040659 REMEDYREPACK INC. MECLIZINE HYDROCHLORIDE 25 mg/1 10 TABLET in 1 BOTTLE, PLASTIC (70518-1308-5)
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