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
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)
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)
71335-0503-0	71335-0503	HUMAN PRESCRIPTION DRUG	MECLIZINE HYDROCHLORIDE	Meclizine Hydrocloride	TABLET	ORAL	20220223	20261031	ANDA	ANDA040659	Bryant Ranch Prepack	MECLIZINE HYDROCHLORIDE	25 mg/1	14 TABLET in 1 BOTTLE (71335-0503-0)
71335-0503-1	71335-0503	HUMAN PRESCRIPTION DRUG	MECLIZINE HYDROCHLORIDE	Meclizine Hydrocloride	TABLET	ORAL	20220223	20261031	ANDA	ANDA040659	Bryant Ranch Prepack	MECLIZINE HYDROCHLORIDE	25 mg/1	90 TABLET in 1 BOTTLE (71335-0503-1)
71335-0503-2	71335-0503	HUMAN PRESCRIPTION DRUG	MECLIZINE HYDROCHLORIDE	Meclizine Hydrocloride	TABLET	ORAL	20220223	20261031	ANDA	ANDA040659	Bryant Ranch Prepack	MECLIZINE HYDROCHLORIDE	25 mg/1	30 TABLET in 1 BOTTLE (71335-0503-2)
71335-0503-3	71335-0503	HUMAN PRESCRIPTION DRUG	MECLIZINE HYDROCHLORIDE	Meclizine Hydrocloride	TABLET	ORAL	20220223	20261031	ANDA	ANDA040659	Bryant Ranch Prepack	MECLIZINE HYDROCHLORIDE	25 mg/1	25 TABLET in 1 BOTTLE (71335-0503-3)
71335-0503-4	71335-0503	HUMAN PRESCRIPTION DRUG	MECLIZINE HYDROCHLORIDE	Meclizine Hydrocloride	TABLET	ORAL	20220223	20261031	ANDA	ANDA040659	Bryant Ranch Prepack	MECLIZINE HYDROCHLORIDE	25 mg/1	20 TABLET in 1 BOTTLE (71335-0503-4)
71335-0503-5	71335-0503	HUMAN PRESCRIPTION DRUG	MECLIZINE HYDROCHLORIDE	Meclizine Hydrocloride	TABLET	ORAL	20220223	20261031	ANDA	ANDA040659	Bryant Ranch Prepack	MECLIZINE HYDROCHLORIDE	25 mg/1	40 TABLET in 1 BOTTLE (71335-0503-5)
71335-0503-6	71335-0503	HUMAN PRESCRIPTION DRUG	MECLIZINE HYDROCHLORIDE	Meclizine Hydrocloride	TABLET	ORAL	20220223	20261031	ANDA	ANDA040659	Bryant Ranch Prepack	MECLIZINE HYDROCHLORIDE	25 mg/1	60 TABLET in 1 BOTTLE (71335-0503-6)
71335-0503-7	71335-0503	HUMAN PRESCRIPTION DRUG	MECLIZINE HYDROCHLORIDE	Meclizine Hydrocloride	TABLET	ORAL	20220223	20261031	ANDA	ANDA040659	Bryant Ranch Prepack	MECLIZINE HYDROCHLORIDE	25 mg/1	120 TABLET in 1 BOTTLE (71335-0503-7)
71335-0503-8	71335-0503	HUMAN PRESCRIPTION DRUG	MECLIZINE HYDROCHLORIDE	Meclizine Hydrocloride	TABLET	ORAL	20220223	20261031	ANDA	ANDA040659	Bryant Ranch Prepack	MECLIZINE HYDROCHLORIDE	25 mg/1	10 TABLET in 1 BOTTLE (71335-0503-8)
71335-0503-9	71335-0503	HUMAN PRESCRIPTION DRUG	MECLIZINE HYDROCHLORIDE	Meclizine Hydrocloride	TABLET	ORAL	20220223	20261031	ANDA	ANDA040659	Bryant Ranch Prepack	MECLIZINE HYDROCHLORIDE	25 mg/1	100 TABLET in 1 BOTTLE (71335-0503-9)