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
68788-8633-1	68788-8633	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET	ORAL	20240416	N/A	NDA AUTHORIZED GENERIC	NDA010721	Preferred Pharmaceuticals Inc.	MECLIZINE HYDROCHLORIDE	12.5 mg/1	10 TABLET in 1 BOTTLE (68788-8633-1)
68788-8633-3	68788-8633	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET	ORAL	20240416	N/A	NDA AUTHORIZED GENERIC	NDA010721	Preferred Pharmaceuticals Inc.	MECLIZINE HYDROCHLORIDE	12.5 mg/1	30 TABLET in 1 BOTTLE (68788-8633-3)
67296-1432-3	67296-1432	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET	ORAL	20210301	N/A	NDA AUTHORIZED GENERIC	NDA010721	RedPharm Drug, Inc.	MECLIZINE HYDROCHLORIDE	25 mg/1	30 TABLET in 1 BOTTLE (67296-1432-3)
67296-1432-7	67296-1432	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET	ORAL	20200115	N/A	NDA AUTHORIZED GENERIC	NDA010721	RedPharm Drug, Inc.	MECLIZINE HYDROCHLORIDE	25 mg/1	21 TABLET in 1 BOTTLE (67296-1432-7)
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)
70199-002-01	70199-002	HUMAN PRESCRIPTION DRUG	Antivert	meclizine HCl	TABLET	ORAL	20200115	N/A	NDA	NDA010721	Casper Pharma LLC	MECLIZINE HYDROCHLORIDE	12.5 mg/1	100 TABLET in 1 BOTTLE (70199-002-01)
70199-002-05	70199-002	HUMAN PRESCRIPTION DRUG	Antivert	meclizine HCl	TABLET	ORAL	20200115	N/A	NDA	NDA010721	Casper Pharma LLC	MECLIZINE HYDROCHLORIDE	12.5 mg/1	500 TABLET in 1 BOTTLE (70199-002-05)
70199-003-01	70199-003	HUMAN PRESCRIPTION DRUG	Antivert	meclizine HCl	TABLET	ORAL	20200115	N/A	NDA	NDA010721	Casper Pharma LLC	MECLIZINE HYDROCHLORIDE	25 mg/1	100 TABLET in 1 BOTTLE (70199-003-01)
70199-003-99	70199-003	HUMAN PRESCRIPTION DRUG	Antivert	meclizine HCl	TABLET	ORAL	20200115	N/A	NDA	NDA010721	Casper Pharma LLC	MECLIZINE HYDROCHLORIDE	25 mg/1	1000 TABLET in 1 BOTTLE (70199-003-99)
70199-004-01	70199-004	HUMAN PRESCRIPTION DRUG	Antivert	meclizine hcl	TABLET	ORAL	20200115	N/A	NDA	NDA010721	Casper Pharma LLC	MECLIZINE HYDROCHLORIDE	50 mg/1	100 TABLET in 1 BOTTLE (70199-004-01)
70199-004-99	70199-004	HUMAN PRESCRIPTION DRUG	Antivert	meclizine hcl	TABLET	ORAL	20200115	N/A	NDA	NDA010721	Casper Pharma LLC	MECLIZINE HYDROCHLORIDE	50 mg/1	1000 TABLET in 1 BOTTLE (70199-004-99)
70199-018-01	70199-018	HUMAN PRESCRIPTION DRUG	Antivert	meclizine hcl	TABLET, CHEWABLE	ORAL	20200115	N/A	NDA	NDA010721	Casper Pharma LLC	MECLIZINE HYDROCHLORIDE	25 mg/1	100 TABLET, CHEWABLE in 1 BOTTLE (70199-018-01)
16571-660-01	16571-660	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET	ORAL	20200115	N/A	NDA AUTHORIZED GENERIC	NDA010721	Rising Pharmaceuticals, Inc.	MECLIZINE HYDROCHLORIDE	12.5 mg/1	100 TABLET in 1 BOTTLE (16571-660-01)
16571-660-50	16571-660	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET	ORAL	20200115	N/A	NDA AUTHORIZED GENERIC	NDA010721	Rising Pharmaceuticals, Inc.	MECLIZINE HYDROCHLORIDE	12.5 mg/1	500 TABLET in 1 BOTTLE (16571-660-50)
16571-661-01	16571-661	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET	ORAL	20200115	N/A	NDA AUTHORIZED GENERIC	NDA010721	Rising Pharmaceuticals, Inc.	MECLIZINE HYDROCHLORIDE	25 mg/1	100 TABLET in 1 BOTTLE (16571-661-01)
16571-661-10	16571-661	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET	ORAL	20200115	N/A	NDA AUTHORIZED GENERIC	NDA010721	Rising Pharmaceuticals, Inc.	MECLIZINE HYDROCHLORIDE	25 mg/1	1000 TABLET in 1 BOTTLE (16571-661-10)
16571-662-01	16571-662	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET	ORAL	20200115	N/A	NDA AUTHORIZED GENERIC	NDA010721	Rising Pharmaceuticals, Inc.	MECLIZINE HYDROCHLORIDE	50 mg/1	100 TABLET in 1 BOTTLE (16571-662-01)
16571-663-01	16571-663	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET, CHEWABLE	ORAL	20200115	N/A	NDA AUTHORIZED GENERIC	NDA010721	Rising Pharmaceuticals, Inc.	MECLIZINE HYDROCHLORIDE	25 mg/1	100 TABLET, CHEWABLE in 1 BOTTLE (16571-663-01)
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)