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
71205-647-10	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)
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)
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)