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
70518-3815-3	70518-3815	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET	ORAL	20250913	N/A	NDA AUTHORIZED GENERIC	NDA010721	REMEDYREPACK INC.	MECLIZINE HYDROCHLORIDE	25 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (70518-3815-3)
70518-3815-4	70518-3815	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET	ORAL	20260112	N/A	NDA AUTHORIZED GENERIC	NDA010721	REMEDYREPACK INC.	MECLIZINE HYDROCHLORIDE	25 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (70518-3815-4)
16571-660-01	16571-660	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET	ORAL	20200115	N/A	NDA AUTHORIZED GENERIC	NDA010721	Rising Pharma Holdings, 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 Pharma Holdings, 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 Pharma Holdings, 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 Pharma Holdings, 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 Pharma Holdings, 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 Pharma Holdings, Inc.	MECLIZINE HYDROCHLORIDE	25 mg/1	100 TABLET, CHEWABLE in 1 BOTTLE (16571-663-01)
80425-0494-1	80425-0494	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET	ORAL	20250202	N/A	NDA AUTHORIZED GENERIC	NDA010721	Advanced Rx of Tennessee, LLC	MECLIZINE HYDROCHLORIDE	25 mg/1	30 TABLET in 1 BOTTLE (80425-0494-1)
80425-0494-2	80425-0494	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET	ORAL	20250202	N/A	NDA AUTHORIZED GENERIC	NDA010721	Advanced Rx of Tennessee, LLC	MECLIZINE HYDROCHLORIDE	25 mg/1	60 TABLET in 1 BOTTLE (80425-0494-2)
80425-0494-3	80425-0494	HUMAN PRESCRIPTION DRUG	Meclizine Hydrochloride	Meclizine Hydrochloride	TABLET	ORAL	20250202	N/A	NDA AUTHORIZED GENERIC	NDA010721	Advanced Rx of Tennessee, LLC	MECLIZINE HYDROCHLORIDE	25 mg/1	90 TABLET in 1 BOTTLE (80425-0494-3)
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)
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)
72189-237-30	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)
72189-237-90	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)
72189-302-30	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)
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)