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=ANDA213957"
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
70771-1540-0 70771-1540 HUMAN PRESCRIPTION DRUG Meclizine Hydrochloride Meclizine Hydrochloride TABLET ORAL 20201029 N/A ANDA ANDA213957 Zydus Lifesciences Limited MECLIZINE HYDROCHLORIDE 25 mg/1 1000 TABLET in 1 BOTTLE (70771-1540-0)
70771-1540-1 70771-1540 HUMAN PRESCRIPTION DRUG Meclizine Hydrochloride Meclizine Hydrochloride TABLET ORAL 20201029 N/A ANDA ANDA213957 Zydus Lifesciences Limited MECLIZINE HYDROCHLORIDE 25 mg/1 100 TABLET in 1 BOTTLE (70771-1540-1)
70771-1540-3 70771-1540 HUMAN PRESCRIPTION DRUG Meclizine Hydrochloride Meclizine Hydrochloride TABLET ORAL 20201029 N/A ANDA ANDA213957 Zydus Lifesciences Limited MECLIZINE HYDROCHLORIDE 25 mg/1 30 TABLET in 1 BOTTLE (70771-1540-3)
70771-1540-4 70771-1540 HUMAN PRESCRIPTION DRUG Meclizine Hydrochloride Meclizine Hydrochloride TABLET ORAL 20201029 N/A ANDA ANDA213957 Zydus Lifesciences Limited MECLIZINE HYDROCHLORIDE 25 mg/1 10 BLISTER PACK in 1 CARTON (70771-1540-4) / 10 TABLET in 1 BLISTER PACK (70771-1540-2)
70771-1540-9 70771-1540 HUMAN PRESCRIPTION DRUG Meclizine Hydrochloride Meclizine Hydrochloride TABLET ORAL 20201029 N/A ANDA ANDA213957 Zydus Lifesciences Limited MECLIZINE HYDROCHLORIDE 25 mg/1 90 TABLET in 1 BOTTLE (70771-1540-9)
67296-2138-2 67296-2138 HUMAN PRESCRIPTION DRUG Meclizine Hydrochloride Meclizine Hydrochloride TABLET ORAL 20201029 N/A ANDA ANDA213957 Redpharm Drug MECLIZINE HYDROCHLORIDE 25 mg/1 21 TABLET in 1 BOTTLE (67296-2138-2)
68071-3748-4 68071-3748 HUMAN PRESCRIPTION DRUG Meclizine Hydrochloride Meclizine Hydrochloride TABLET ORAL 20250515 N/A ANDA ANDA213957 NuCare Pharmaceuticals, Inc. MECLIZINE HYDROCHLORIDE 25 mg/1 4 TABLET in 1 BOTTLE (68071-3748-4)
68071-3748-6 68071-3748 HUMAN PRESCRIPTION DRUG Meclizine Hydrochloride Meclizine Hydrochloride TABLET ORAL 20241218 N/A ANDA ANDA213957 NuCare Pharmaceuticals, Inc. MECLIZINE HYDROCHLORIDE 25 mg/1 6 TABLET in 1 BOTTLE (68071-3748-6)
68071-3791-2 68071-3791 HUMAN PRESCRIPTION DRUG Meclizine Hydrochloride Meclizine Hydrochloride TABLET ORAL 20250213 N/A ANDA ANDA213957 NuCare Pharmaceuticals, Inc. MECLIZINE HYDROCHLORIDE 25 mg/1 20 TABLET in 1 BOTTLE (68071-3791-2)
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