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
71335-0153-1 71335-0153 HUMAN PRESCRIPTION DRUG MECLIZINE HYDROCHLORIDE Meclizine Hydrochloride TABLET ORAL 20220223 20261031 ANDA ANDA040659 Bryant Ranch Prepack MECLIZINE HYDROCHLORIDE 12.5 mg/1 30 TABLET in 1 BOTTLE (71335-0153-1)
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)
71335-0153-3 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)
71335-0153-5 71335-0153 HUMAN PRESCRIPTION DRUG MECLIZINE HYDROCHLORIDE Meclizine Hydrochloride TABLET ORAL 20220223 20261031 ANDA ANDA040659 Bryant Ranch Prepack MECLIZINE HYDROCHLORIDE 12.5 mg/1 20 TABLET in 1 BOTTLE (71335-0153-5)
71335-0153-6 71335-0153 HUMAN PRESCRIPTION DRUG MECLIZINE HYDROCHLORIDE Meclizine Hydrochloride TABLET ORAL 20220223 20261031 ANDA ANDA040659 Bryant Ranch Prepack MECLIZINE HYDROCHLORIDE 12.5 mg/1 120 TABLET in 1 BOTTLE (71335-0153-6)
71335-0153-7 71335-0153 HUMAN PRESCRIPTION DRUG MECLIZINE HYDROCHLORIDE Meclizine Hydrochloride TABLET ORAL 20220223 20261031 ANDA ANDA040659 Bryant Ranch Prepack MECLIZINE HYDROCHLORIDE 12.5 mg/1 100 TABLET in 1 BOTTLE (71335-0153-7)
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)
42708-102-30 42708-102 HUMAN PRESCRIPTION DRUG Meclizine Hydrocloride Meclizine Hydrocloride TABLET ORAL 20191018 20261031 ANDA ANDA040659 QPharma Inc MECLIZINE HYDROCHLORIDE 25 mg/1 30 TABLET in 1 BOTTLE (42708-102-30)
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)
71335-0503-1 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)
51655-107-20 51655-107 HUMAN PRESCRIPTION DRUG MECLIZINE HYDROCHLORIDE MECLIZINE HYDROCHLORIDE TABLET ORAL 20231214 20261031 ANDA ANDA040659 Northwind Health Company, LLC MECLIZINE HYDROCHLORIDE 25 mg/1 20 TABLET in 1 BOTTLE, PLASTIC (51655-107-20)
51655-107-52 51655-107 HUMAN PRESCRIPTION DRUG MECLIZINE HYDROCHLORIDE MECLIZINE HYDROCHLORIDE TABLET ORAL 20140724 20261031 ANDA ANDA040659 Northwind Health Company, LLC MECLIZINE HYDROCHLORIDE 25 mg/1 30 TABLET in 1 BOTTLE, DISPENSING (51655-107-52)
59746-122-06 59746-122 HUMAN PRESCRIPTION DRUG MECLIZINE HYDROCHLORIDE Meclizine Hydrochloride TABLET ORAL 20100604 20261031 ANDA ANDA040659 Jubilant Cadista Pharmacuticals Inc. MECLIZINE HYDROCHLORIDE 12.5 mg/1 100 TABLET in 1 BOTTLE (59746-122-06)
59746-122-10 59746-122 HUMAN PRESCRIPTION DRUG MECLIZINE HYDROCHLORIDE Meclizine Hydrochloride TABLET ORAL 20100604 20261031 ANDA ANDA040659 Jubilant Cadista Pharmacuticals Inc. MECLIZINE HYDROCHLORIDE 12.5 mg/1 1000 TABLET in 1 BOTTLE (59746-122-10)
68071-3017-1 68071-3017 HUMAN PRESCRIPTION DRUG MECLIZINE HYDROCHLORIDE Meclizine Hydrocloride TABLET ORAL 20180207 N/A ANDA ANDA040659 NuCare Pharmaceuticals,Inc. MECLIZINE HYDROCHLORIDE 25 mg/1 12 TABLET in 1 BOTTLE (68071-3017-1)
68071-3017-2 68071-3017 HUMAN PRESCRIPTION DRUG MECLIZINE HYDROCHLORIDE Meclizine Hydrocloride TABLET ORAL 20180207 N/A ANDA ANDA040659 NuCare Pharmaceuticals,Inc. MECLIZINE HYDROCHLORIDE 25 mg/1 20 TABLET in 1 BOTTLE (68071-3017-2)
68071-3017-3 68071-3017 HUMAN PRESCRIPTION DRUG MECLIZINE HYDROCHLORIDE Meclizine Hydrocloride TABLET ORAL 20180207 N/A ANDA ANDA040659 NuCare Pharmaceuticals,Inc. MECLIZINE HYDROCHLORIDE 25 mg/1 30 TABLET in 1 BOTTLE (68071-3017-3)
68071-3017-6 68071-3017 HUMAN PRESCRIPTION DRUG MECLIZINE HYDROCHLORIDE Meclizine Hydrocloride TABLET ORAL 20180207 N/A ANDA ANDA040659 NuCare Pharmaceuticals,Inc. MECLIZINE HYDROCHLORIDE 25 mg/1 60 TABLET in 1 BOTTLE (68071-3017-6)
68071-3017-7 68071-3017 HUMAN PRESCRIPTION DRUG MECLIZINE HYDROCHLORIDE Meclizine Hydrocloride TABLET ORAL 20180207 N/A ANDA ANDA040659 NuCare Pharmaceuticals,Inc. MECLIZINE HYDROCHLORIDE 25 mg/1 10 TABLET in 1 BOTTLE (68071-3017-7)
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