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
71335-0503-3	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)
63629-2432-1	63629-2432	HUMAN PRESCRIPTION DRUG	MECLIZINE HYDROCHLORIDE	Meclizine Hydrochloride	TABLET	ORAL	20210225	20261031	ANDA	ANDA040659	Bryant Ranch Prepack	MECLIZINE HYDROCHLORIDE	12.5 mg/1	1000 TABLET in 1 BOTTLE (63629-2432-1)
72162-1690-0	72162-1690	HUMAN PRESCRIPTION DRUG	MECLIZINE HYDROCHLORIDE	Meclizine Hydrochloride	TABLET	ORAL	20230912	20261031	ANDA	ANDA040659	Bryant Ranch Prepack	MECLIZINE HYDROCHLORIDE	12.5 mg/1	1000 TABLET in 1 BOTTLE (72162-1690-0)
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)
70518-1308-0	70518-1308	HUMAN PRESCRIPTION DRUG	MECLIZINE HYDROCHLORIDE	Meclizine Hydrocloride	TABLET	ORAL	20180817	20261031	ANDA	ANDA040659	REMEDYREPACK INC.	MECLIZINE HYDROCHLORIDE	25 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (70518-1308-0)
76420-130-20	76420-130	HUMAN PRESCRIPTION DRUG	MECLIZINE HYDROCHLORIDE	Meclizine Hydrocloride	TABLET	ORAL	20201030	N/A	ANDA	ANDA040659	Asclemed USA, Inc.	MECLIZINE HYDROCHLORIDE	25 mg/1	20 TABLET in 1 BOTTLE (76420-130-20)
76420-130-30	76420-130	HUMAN PRESCRIPTION DRUG	MECLIZINE HYDROCHLORIDE	Meclizine Hydrocloride	TABLET	ORAL	20201030	N/A	ANDA	ANDA040659	Asclemed USA, Inc.	MECLIZINE HYDROCHLORIDE	25 mg/1	30 TABLET in 1 BOTTLE (76420-130-30)
76420-130-10	76420-130	HUMAN PRESCRIPTION DRUG	MECLIZINE HYDROCHLORIDE	Meclizine Hydrocloride	TABLET	ORAL	20201030	N/A	ANDA	ANDA040659	Asclemed USA, Inc.	MECLIZINE HYDROCHLORIDE	25 mg/1	10 TABLET in 1 BOTTLE (76420-130-10)
70518-1308-5	70518-1308	HUMAN PRESCRIPTION DRUG	MECLIZINE HYDROCHLORIDE	Meclizine Hydrocloride	TABLET	ORAL	20231218	20261031	ANDA	ANDA040659	REMEDYREPACK INC.	MECLIZINE HYDROCHLORIDE	25 mg/1	10 TABLET in 1 BOTTLE, PLASTIC (70518-1308-5)