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
16571-663-01	16571-663	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET, CHEWABLE	ORAL	20200115	N/A	NDA AUTHORIZED GENERIC	NDA010721	Rising Pharma Holdings, Inc.	MECLIZINE HYDROCHLORIDE	25 mg/1	100 TABLET, CHEWABLE in 1 BOTTLE (16571-663-01)
71205-647-10	71205-647	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET	ORAL	20220323	N/A	NDA AUTHORIZED GENERIC	NDA010721	Proficient Rx LP	MECLIZINE HYDROCHLORIDE	12.5 mg/1	10 TABLET in 1 BOTTLE (71205-647-10)
71205-647-90	71205-647	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET	ORAL	20220323	N/A	NDA AUTHORIZED GENERIC	NDA010721	Proficient Rx LP	MECLIZINE HYDROCHLORIDE	12.5 mg/1	90 TABLET in 1 BOTTLE (71205-647-90)
70518-3815-1	70518-3815	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET	ORAL	20240406	N/A	NDA AUTHORIZED GENERIC	NDA010721	REMEDYREPACK INC.	MECLIZINE HYDROCHLORIDE	25 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (70518-3815-1)
70518-3815-2	70518-3815	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET	ORAL	20250207	N/A	NDA AUTHORIZED GENERIC	NDA010721	REMEDYREPACK INC.	MECLIZINE HYDROCHLORIDE	25 mg/1	30 TABLET in 1 BLISTER PACK (70518-3815-2)
70518-3815-3	70518-3815	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET	ORAL	20250913	N/A	NDA AUTHORIZED GENERIC	NDA010721	REMEDYREPACK INC.	MECLIZINE HYDROCHLORIDE	25 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (70518-3815-3)
70518-3815-4	70518-3815	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET	ORAL	20260112	N/A	NDA AUTHORIZED GENERIC	NDA010721	REMEDYREPACK INC.	MECLIZINE HYDROCHLORIDE	25 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (70518-3815-4)
70518-3815-5	70518-3815	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET	ORAL	20260217	N/A	NDA AUTHORIZED GENERIC	NDA010721	REMEDYREPACK INC.	MECLIZINE HYDROCHLORIDE	25 mg/1	10 TABLET in 1 BOTTLE, PLASTIC (70518-3815-5)
72189-237-30	72189-237	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET	ORAL	20220901	N/A	NDA AUTHORIZED GENERIC	NDA010721	Direct_Rx	MECLIZINE HYDROCHLORIDE	25 mg/1	30 TABLET in 1 BOTTLE (72189-237-30)
72189-237-90	72189-237	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET	ORAL	20220901	N/A	NDA AUTHORIZED GENERIC	NDA010721	Direct_Rx	MECLIZINE HYDROCHLORIDE	25 mg/1	90 TABLET in 1 BOTTLE (72189-237-90)
16571-662-01	16571-662	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET	ORAL	20200115	N/A	NDA AUTHORIZED GENERIC	NDA010721	Rising Pharma Holdings, Inc.	MECLIZINE HYDROCHLORIDE	50 mg/1	100 TABLET in 1 BOTTLE (16571-662-01)
70518-3768-0	70518-3768	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET	ORAL	20230619	N/A	NDA AUTHORIZED GENERIC	NDA010721	REMEDYREPACK INC.	MECLIZINE HYDROCHLORIDE	12.5 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (70518-3768-0)
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)
71335-1825-1	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)
71335-1825-2	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)
71335-1825-3	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)