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）

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
71335-1825-3	71335-1825	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET	ORAL	20220224	N/A	NDA AUTHORIZED GENERIC	NDA010721	Bryant Ranch Prepack	MECLIZINE HYDROCHLORIDE	25 mg/1	25 TABLET in 1 BOTTLE (71335-1825-3)
71335-1825-4	71335-1825	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET	ORAL	20220224	N/A	NDA AUTHORIZED GENERIC	NDA010721	Bryant Ranch Prepack	MECLIZINE HYDROCHLORIDE	25 mg/1	20 TABLET in 1 BOTTLE (71335-1825-4)
71335-1825-5	71335-1825	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET	ORAL	20220224	N/A	NDA AUTHORIZED GENERIC	NDA010721	Bryant Ranch Prepack	MECLIZINE HYDROCHLORIDE	25 mg/1	40 TABLET in 1 BOTTLE (71335-1825-5)
71335-1825-6	71335-1825	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET	ORAL	20220224	N/A	NDA AUTHORIZED GENERIC	NDA010721	Bryant Ranch Prepack	MECLIZINE HYDROCHLORIDE	25 mg/1	60 TABLET in 1 BOTTLE (71335-1825-6)
71335-1825-7	71335-1825	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET	ORAL	20220224	N/A	NDA AUTHORIZED GENERIC	NDA010721	Bryant Ranch Prepack	MECLIZINE HYDROCHLORIDE	25 mg/1	120 TABLET in 1 BOTTLE (71335-1825-7)
71335-1825-8	71335-1825	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET	ORAL	20220224	N/A	NDA AUTHORIZED GENERIC	NDA010721	Bryant Ranch Prepack	MECLIZINE HYDROCHLORIDE	25 mg/1	10 TABLET in 1 BOTTLE (71335-1825-8)
71335-1825-9	71335-1825	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET	ORAL	20220224	N/A	NDA AUTHORIZED GENERIC	NDA010721	Bryant Ranch Prepack	MECLIZINE HYDROCHLORIDE	25 mg/1	100 TABLET in 1 BOTTLE (71335-1825-9)
71335-1825-2	71335-1825	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET	ORAL	20220224	N/A	NDA AUTHORIZED GENERIC	NDA010721	Bryant Ranch Prepack	MECLIZINE HYDROCHLORIDE	25 mg/1	30 TABLET in 1 BOTTLE (71335-1825-2)
71335-1825-1	71335-1825	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET	ORAL	20220224	N/A	NDA AUTHORIZED GENERIC	NDA010721	Bryant Ranch Prepack	MECLIZINE HYDROCHLORIDE	25 mg/1	90 TABLET in 1 BOTTLE (71335-1825-1)
71335-1825-0	71335-1825	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET	ORAL	20220224	N/A	NDA AUTHORIZED GENERIC	NDA010721	Bryant Ranch Prepack	MECLIZINE HYDROCHLORIDE	25 mg/1	14 TABLET in 1 BOTTLE (71335-1825-0)
71335-1872-1	71335-1872	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET	ORAL	20210628	N/A	NDA AUTHORIZED GENERIC	NDA010721	Bryant Ranch Prepack	MECLIZINE HYDROCHLORIDE	12.5 mg/1	30 TABLET in 1 BOTTLE (71335-1872-1)
71335-1872-5	71335-1872	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET	ORAL	20210628	N/A	NDA AUTHORIZED GENERIC	NDA010721	Bryant Ranch Prepack	MECLIZINE HYDROCHLORIDE	12.5 mg/1	20 TABLET in 1 BOTTLE (71335-1872-5)
71335-1872-6	71335-1872	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET	ORAL	20210628	N/A	NDA AUTHORIZED GENERIC	NDA010721	Bryant Ranch Prepack	MECLIZINE HYDROCHLORIDE	12.5 mg/1	120 TABLET in 1 BOTTLE (71335-1872-6)
71335-1872-7	71335-1872	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET	ORAL	20210628	N/A	NDA AUTHORIZED GENERIC	NDA010721	Bryant Ranch Prepack	MECLIZINE HYDROCHLORIDE	12.5 mg/1	100 TABLET in 1 BOTTLE (71335-1872-7)
71335-1872-8	71335-1872	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET	ORAL	20210628	N/A	NDA AUTHORIZED GENERIC	NDA010721	Bryant Ranch Prepack	MECLIZINE HYDROCHLORIDE	12.5 mg/1	10 TABLET in 1 BOTTLE (71335-1872-8)
76420-797-01	76420-797	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET	ORAL	20240405	N/A	NDA AUTHORIZED GENERIC	NDA010721	Asclemed USA, Inc.	MECLIZINE HYDROCHLORIDE	12.5 mg/1	100 TABLET in 1 BOTTLE (76420-797-01)
76420-797-30	76420-797	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET	ORAL	20240405	N/A	NDA AUTHORIZED GENERIC	NDA010721	Asclemed USA, Inc.	MECLIZINE HYDROCHLORIDE	12.5 mg/1	30 TABLET in 1 BOTTLE (76420-797-30)
76420-797-60	76420-797	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET	ORAL	20240405	N/A	NDA AUTHORIZED GENERIC	NDA010721	Asclemed USA, Inc.	MECLIZINE HYDROCHLORIDE	12.5 mg/1	60 TABLET in 1 BOTTLE (76420-797-60)
76420-797-90	76420-797	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET	ORAL	20240405	N/A	NDA AUTHORIZED GENERIC	NDA010721	Asclemed USA, Inc.	MECLIZINE HYDROCHLORIDE	12.5 mg/1	90 TABLET in 1 BOTTLE (76420-797-90)
76420-798-01	76420-798	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET	ORAL	20240405	N/A	NDA AUTHORIZED GENERIC	NDA010721	Asclemed USA, Inc.	MECLIZINE HYDROCHLORIDE	25 mg/1	100 TABLET in 1 BOTTLE (76420-798-01)