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
51655-107-20	51655-107	HUMAN PRESCRIPTION DRUG	MECLIZINE HYDROCHLORIDE	MECLIZINE HYDROCHLORIDE	TABLET	ORAL	20231214	20261031	ANDA	ANDA040659	Northwind Health Company, 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	20261031	ANDA	ANDA040659	Northwind Health Company, LLC	MECLIZINE HYDROCHLORIDE	25 mg/1	30 TABLET in 1 BOTTLE, DISPENSING (51655-107-52)
60760-087-90	60760-087	HUMAN PRESCRIPTION DRUG	MECLIZINE HYDROCHLORIDE	Meclizine Hydrocloride	TABLET	ORAL	20190418	N/A	ANDA	ANDA040659	St. Mary's Medical Park Pharmacy	MECLIZINE HYDROCHLORIDE	25 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (60760-087-90)
71335-0153-1	71335-0153	HUMAN PRESCRIPTION DRUG	MECLIZINE HYDROCHLORIDE	Meclizine Hydrochloride	TABLET	ORAL	20220223	20261031	ANDA	ANDA040659	Bryant Ranch Prepack	MECLIZINE HYDROCHLORIDE	12.5 mg/1	30 TABLET in 1 BOTTLE (71335-0153-1)
71335-0153-2	71335-0153	HUMAN PRESCRIPTION DRUG	MECLIZINE HYDROCHLORIDE	Meclizine Hydrochloride	TABLET	ORAL	20220223	20261031	ANDA	ANDA040659	Bryant Ranch Prepack	MECLIZINE HYDROCHLORIDE	12.5 mg/1	60 TABLET in 1 BOTTLE (71335-0153-2)
71335-0153-3	71335-0153	HUMAN PRESCRIPTION DRUG	MECLIZINE HYDROCHLORIDE	Meclizine Hydrochloride	TABLET	ORAL	20220223	20261031	ANDA	ANDA040659	Bryant Ranch Prepack	MECLIZINE HYDROCHLORIDE	12.5 mg/1	90 TABLET in 1 BOTTLE (71335-0153-3)
71335-0153-4	71335-0153	HUMAN PRESCRIPTION DRUG	MECLIZINE HYDROCHLORIDE	Meclizine Hydrochloride	TABLET	ORAL	20220223	20261031	ANDA	ANDA040659	Bryant Ranch Prepack	MECLIZINE HYDROCHLORIDE	12.5 mg/1	28 TABLET in 1 BOTTLE (71335-0153-4)
71335-0153-5	71335-0153	HUMAN PRESCRIPTION DRUG	MECLIZINE HYDROCHLORIDE	Meclizine Hydrochloride	TABLET	ORAL	20220223	20261031	ANDA	ANDA040659	Bryant Ranch Prepack	MECLIZINE HYDROCHLORIDE	12.5 mg/1	20 TABLET in 1 BOTTLE (71335-0153-5)
71335-0153-6	71335-0153	HUMAN PRESCRIPTION DRUG	MECLIZINE HYDROCHLORIDE	Meclizine Hydrochloride	TABLET	ORAL	20220223	20261031	ANDA	ANDA040659	Bryant Ranch Prepack	MECLIZINE HYDROCHLORIDE	12.5 mg/1	120 TABLET in 1 BOTTLE (71335-0153-6)
71335-0153-7	71335-0153	HUMAN PRESCRIPTION DRUG	MECLIZINE HYDROCHLORIDE	Meclizine Hydrochloride	TABLET	ORAL	20220223	20261031	ANDA	ANDA040659	Bryant Ranch Prepack	MECLIZINE HYDROCHLORIDE	12.5 mg/1	100 TABLET in 1 BOTTLE (71335-0153-7)
71335-0153-8	71335-0153	HUMAN PRESCRIPTION DRUG	MECLIZINE HYDROCHLORIDE	Meclizine Hydrochloride	TABLET	ORAL	20250911	20261031	ANDA	ANDA040659	Bryant Ranch Prepack	MECLIZINE HYDROCHLORIDE	12.5 mg/1	10 TABLET in 1 BOTTLE (71335-0153-8)
71205-416-10	71205-416	HUMAN PRESCRIPTION DRUG	MECLIZINE HYDROCHLORIDE	Meclizine Hydrochloride	TABLET	ORAL	20200303	N/A	ANDA	ANDA040659	Proficient Rx LP	MECLIZINE HYDROCHLORIDE	12.5 mg/1	10 TABLET in 1 BOTTLE (71205-416-10)
71205-416-30	71205-416	HUMAN PRESCRIPTION DRUG	MECLIZINE HYDROCHLORIDE	Meclizine Hydrochloride	TABLET	ORAL	20200303	N/A	ANDA	ANDA040659	Proficient Rx LP	MECLIZINE HYDROCHLORIDE	12.5 mg/1	30 TABLET in 1 BOTTLE (71205-416-30)
71205-416-60	71205-416	HUMAN PRESCRIPTION DRUG	MECLIZINE HYDROCHLORIDE	Meclizine Hydrochloride	TABLET	ORAL	20200303	N/A	ANDA	ANDA040659	Proficient Rx LP	MECLIZINE HYDROCHLORIDE	12.5 mg/1	60 TABLET in 1 BOTTLE (71205-416-60)
71205-416-90	71205-416	HUMAN PRESCRIPTION DRUG	MECLIZINE HYDROCHLORIDE	Meclizine Hydrochloride	TABLET	ORAL	20200303	N/A	ANDA	ANDA040659	Proficient Rx LP	MECLIZINE HYDROCHLORIDE	12.5 mg/1	90 TABLET in 1 BOTTLE (71205-416-90)