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
70710-1161-1	70710-1161	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET	ORAL	20201029	N/A	ANDA	ANDA213957	Zydus Pharmaceuticals (USA) Inc.	MECLIZINE HYDROCHLORIDE	12.5 mg/1	100 TABLET in 1 BOTTLE (70710-1161-1)
70710-1161-3	70710-1161	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET	ORAL	20201029	N/A	ANDA	ANDA213957	Zydus Pharmaceuticals (USA) Inc.	MECLIZINE HYDROCHLORIDE	12.5 mg/1	30 TABLET in 1 BOTTLE (70710-1161-3)
70710-1161-4	70710-1161	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET	ORAL	20201029	N/A	ANDA	ANDA213957	Zydus Pharmaceuticals (USA) Inc.	MECLIZINE HYDROCHLORIDE	12.5 mg/1	10 BLISTER PACK in 1 CARTON (70710-1161-4) / 10 TABLET in 1 BLISTER PACK (70710-1161-2)
70710-1161-9	70710-1161	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET	ORAL	20201029	N/A	ANDA	ANDA213957	Zydus Pharmaceuticals (USA) Inc.	MECLIZINE HYDROCHLORIDE	12.5 mg/1	90 TABLET in 1 BOTTLE (70710-1161-9)
50090-5727-2	50090-5727	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET	ORAL	20210928	N/A	ANDA	ANDA213957	A-S Medication Solutions	MECLIZINE HYDROCHLORIDE	25 mg/1	12 TABLET in 1 BOTTLE (50090-5727-2)