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
71205-786-30	71205-786	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET	ORAL	20230403	N/A	NDA AUTHORIZED GENERIC	NDA010721	Proficient Rx LP	MECLIZINE HYDROCHLORIDE	25 mg/1	30 TABLET in 1 BOTTLE (71205-786-30)
71205-786-60	71205-786	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET	ORAL	20230403	N/A	NDA AUTHORIZED GENERIC	NDA010721	Proficient Rx LP	MECLIZINE HYDROCHLORIDE	25 mg/1	60 TABLET in 1 BOTTLE (71205-786-60)
71205-786-90	71205-786	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET	ORAL	20230403	N/A	NDA AUTHORIZED GENERIC	NDA010721	Proficient Rx LP	MECLIZINE HYDROCHLORIDE	25 mg/1	90 TABLET in 1 BOTTLE (71205-786-90)
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)
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)
80425-0494-1	80425-0494	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET	ORAL	20250202	N/A	NDA AUTHORIZED GENERIC	NDA010721	Advanced Rx of Tennessee, LLC	MECLIZINE HYDROCHLORIDE	25 mg/1	30 TABLET in 1 BOTTLE (80425-0494-1)
80425-0494-2	80425-0494	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET	ORAL	20250202	N/A	NDA AUTHORIZED GENERIC	NDA010721	Advanced Rx of Tennessee, LLC	MECLIZINE HYDROCHLORIDE	25 mg/1	60 TABLET in 1 BOTTLE (80425-0494-2)
80425-0494-3	80425-0494	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET	ORAL	20250202	N/A	NDA AUTHORIZED GENERIC	NDA010721	Advanced Rx of Tennessee, LLC	MECLIZINE HYDROCHLORIDE	25 mg/1	90 TABLET in 1 BOTTLE (80425-0494-3)
16571-660-01	16571-660	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET	ORAL	20200115	N/A	NDA AUTHORIZED GENERIC	NDA010721	Rising Pharma Holdings, Inc.	MECLIZINE HYDROCHLORIDE	12.5 mg/1	100 TABLET in 1 BOTTLE (16571-660-01)
16571-660-50	16571-660	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET	ORAL	20200115	N/A	NDA AUTHORIZED GENERIC	NDA010721	Rising Pharma Holdings, Inc.	MECLIZINE HYDROCHLORIDE	12.5 mg/1	500 TABLET in 1 BOTTLE (16571-660-50)
16571-661-01	16571-661	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET	ORAL	20200115	N/A	NDA AUTHORIZED GENERIC	NDA010721	Rising Pharma Holdings, Inc.	MECLIZINE HYDROCHLORIDE	25 mg/1	100 TABLET in 1 BOTTLE (16571-661-01)
16571-661-10	16571-661	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET	ORAL	20200115	N/A	NDA AUTHORIZED GENERIC	NDA010721	Rising Pharma Holdings, Inc.	MECLIZINE HYDROCHLORIDE	25 mg/1	1000 TABLET in 1 BOTTLE (16571-661-10)
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)
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)
68788-8633-1	68788-8633	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET	ORAL	20240416	N/A	NDA AUTHORIZED GENERIC	NDA010721	Preferred Pharmaceuticals Inc.	MECLIZINE HYDROCHLORIDE	12.5 mg/1	10 TABLET in 1 BOTTLE (68788-8633-1)
68788-8633-3	68788-8633	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET	ORAL	20240416	N/A	NDA AUTHORIZED GENERIC	NDA010721	Preferred Pharmaceuticals Inc.	MECLIZINE HYDROCHLORIDE	12.5 mg/1	30 TABLET in 1 BOTTLE (68788-8633-3)