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
60760-661-30	60760-661	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET	ORAL	20210621	N/A	NDA AUTHORIZED GENERIC	NDA010721	St. Mary's Medical Park Pharmacy	MECLIZINE HYDROCHLORIDE	25 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (60760-661-30)
60760-661-90	60760-661	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET	ORAL	20220201	N/A	NDA AUTHORIZED GENERIC	NDA010721	St. Mary's Medical Park Pharmacy	MECLIZINE HYDROCHLORIDE	25 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (60760-661-90)
72189-237-90	72189-237	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET	ORAL	20220901	N/A	NDA AUTHORIZED GENERIC	NDA010721	Direct_Rx	MECLIZINE HYDROCHLORIDE	25 mg/1	90 TABLET in 1 BOTTLE (72189-237-90)
72189-237-30	72189-237	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET	ORAL	20220901	N/A	NDA AUTHORIZED GENERIC	NDA010721	Direct_Rx	MECLIZINE HYDROCHLORIDE	25 mg/1	30 TABLET in 1 BOTTLE (72189-237-30)
72189-302-60	72189-302	HUMAN PRESCRIPTION DRUG	MECLIZINE HYDROCHLORIDE	MECLIZINE HYDROCHLORIDE	TABLET	ORAL	20211206	N/A	NDA AUTHORIZED GENERIC	NDA010721	DirectRx	MECLIZINE HYDROCHLORIDE	12.5 mg/1	60 TABLET in 1 BOTTLE (72189-302-60)
72189-302-30	72189-302	HUMAN PRESCRIPTION DRUG	MECLIZINE HYDROCHLORIDE	MECLIZINE HYDROCHLORIDE	TABLET	ORAL	20211206	N/A	NDA AUTHORIZED GENERIC	NDA010721	DirectRx	MECLIZINE HYDROCHLORIDE	12.5 mg/1	30 TABLET in 1 BOTTLE (72189-302-30)
71335-1825-2	71335-1825	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET	ORAL	20220224	N/A	NDA AUTHORIZED GENERIC	NDA010721	Bryant Ranch Prepack	MECLIZINE HYDROCHLORIDE	25 mg/1	30 TABLET in 1 BOTTLE (71335-1825-2)
71335-1825-4	71335-1825	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET	ORAL	20220224	N/A	NDA AUTHORIZED GENERIC	NDA010721	Bryant Ranch Prepack	MECLIZINE HYDROCHLORIDE	25 mg/1	20 TABLET in 1 BOTTLE (71335-1825-4)
71335-1825-5	71335-1825	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET	ORAL	20220224	N/A	NDA AUTHORIZED GENERIC	NDA010721	Bryant Ranch Prepack	MECLIZINE HYDROCHLORIDE	25 mg/1	40 TABLET in 1 BOTTLE (71335-1825-5)
71335-1825-6	71335-1825	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET	ORAL	20220224	N/A	NDA AUTHORIZED GENERIC	NDA010721	Bryant Ranch Prepack	MECLIZINE HYDROCHLORIDE	25 mg/1	60 TABLET in 1 BOTTLE (71335-1825-6)
71335-1825-7	71335-1825	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET	ORAL	20220224	N/A	NDA AUTHORIZED GENERIC	NDA010721	Bryant Ranch Prepack	MECLIZINE HYDROCHLORIDE	25 mg/1	120 TABLET in 1 BOTTLE (71335-1825-7)
71335-1825-8	71335-1825	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET	ORAL	20220224	N/A	NDA AUTHORIZED GENERIC	NDA010721	Bryant Ranch Prepack	MECLIZINE HYDROCHLORIDE	25 mg/1	10 TABLET in 1 BOTTLE (71335-1825-8)
71335-1825-9	71335-1825	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET	ORAL	20220224	N/A	NDA AUTHORIZED GENERIC	NDA010721	Bryant Ranch Prepack	MECLIZINE HYDROCHLORIDE	25 mg/1	100 TABLET in 1 BOTTLE (71335-1825-9)
71335-1825-3	71335-1825	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET	ORAL	20220224	N/A	NDA AUTHORIZED GENERIC	NDA010721	Bryant Ranch Prepack	MECLIZINE HYDROCHLORIDE	25 mg/1	25 TABLET in 1 BOTTLE (71335-1825-3)
71335-1825-0	71335-1825	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET	ORAL	20220224	N/A	NDA AUTHORIZED GENERIC	NDA010721	Bryant Ranch Prepack	MECLIZINE HYDROCHLORIDE	25 mg/1	14 TABLET in 1 BOTTLE (71335-1825-0)
71335-1825-1	71335-1825	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET	ORAL	20220224	N/A	NDA AUTHORIZED GENERIC	NDA010721	Bryant Ranch Prepack	MECLIZINE HYDROCHLORIDE	25 mg/1	90 TABLET in 1 BOTTLE (71335-1825-1)
76420-797-01	76420-797	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET	ORAL	20240405	N/A	NDA AUTHORIZED GENERIC	NDA010721	Asclemed USA, Inc.	MECLIZINE HYDROCHLORIDE	12.5 mg/1	100 TABLET in 1 BOTTLE (76420-797-01)
76420-798-01	76420-798	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET	ORAL	20240405	N/A	NDA AUTHORIZED GENERIC	NDA010721	Asclemed USA, Inc.	MECLIZINE HYDROCHLORIDE	25 mg/1	100 TABLET in 1 BOTTLE (76420-798-01)
76420-798-30	76420-798	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET	ORAL	20240405	N/A	NDA AUTHORIZED GENERIC	NDA010721	Asclemed USA, Inc.	MECLIZINE HYDROCHLORIDE	25 mg/1	30 TABLET in 1 BOTTLE (76420-798-30)
76420-798-60	76420-798	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET	ORAL	20240405	N/A	NDA AUTHORIZED GENERIC	NDA010721	Asclemed USA, Inc.	MECLIZINE HYDROCHLORIDE	25 mg/1	60 TABLET in 1 BOTTLE (76420-798-60)