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
63187-996-90	63187-996	HUMAN PRESCRIPTION DRUG	MECLIZINE HYDROCHLORIDE	Meclizine Hydrocloride	TABLET	ORAL	20220617	N/A	ANDA	ANDA040659	Proficient Rx LP	MECLIZINE HYDROCHLORIDE	25 mg/1	90 TABLET in 1 BOTTLE (63187-996-90)
51655-107-20	51655-107	HUMAN PRESCRIPTION DRUG	MECLIZINE HYDROCHLORIDE	MECLIZINE HYDROCHLORIDE	TABLET	ORAL	20231214	N/A	ANDA	ANDA040659	Northwind Pharmaceuticals, LLC	MECLIZINE HYDROCHLORIDE	25 mg/1	20 TABLET in 1 BOTTLE, PLASTIC (51655-107-20)
51655-107-52	51655-107	HUMAN PRESCRIPTION DRUG	MECLIZINE HYDROCHLORIDE	MECLIZINE HYDROCHLORIDE	TABLET	ORAL	20140724	N/A	ANDA	ANDA040659	Northwind Pharmaceuticals, LLC	MECLIZINE HYDROCHLORIDE	25 mg/1	30 TABLET in 1 BOTTLE, DISPENSING (51655-107-52)