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
11534-204-01	11534-204	HUMAN PRESCRIPTION DRUG	HYDROXYZINE HYDROCHLORIDE	hydroxyzine hydrochloride	TABLET, FILM COATED	ORAL	20240416	N/A	ANDA	ANDA207121	Sunrise Pharmaceutical, Inc.	HYDROXYZINE DIHYDROCHLORIDE	10 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (11534-204-01)
11534-204-03	11534-204	HUMAN PRESCRIPTION DRUG	HYDROXYZINE HYDROCHLORIDE	hydroxyzine hydrochloride	TABLET, FILM COATED	ORAL	20240416	N/A	ANDA	ANDA207121	Sunrise Pharmaceutical, Inc.	HYDROXYZINE DIHYDROCHLORIDE	10 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (11534-204-03)
11534-205-01	11534-205	HUMAN PRESCRIPTION DRUG	HYDROXYZINE HYDROCHLORIDE	hydroxyzine hydrochloride	TABLET, FILM COATED	ORAL	20240506	N/A	ANDA	ANDA207121	Sunrise Pharmaceutical, Inc.	HYDROXYZINE DIHYDROCHLORIDE	25 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (11534-205-01)
11534-205-03	11534-205	HUMAN PRESCRIPTION DRUG	HYDROXYZINE HYDROCHLORIDE	hydroxyzine hydrochloride	TABLET, FILM COATED	ORAL	20240506	N/A	ANDA	ANDA207121	Sunrise Pharmaceutical, Inc.	HYDROXYZINE DIHYDROCHLORIDE	25 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (11534-205-03)
11534-206-01	11534-206	HUMAN PRESCRIPTION DRUG	HYDROXYZINE HYDROCHLORIDE	hydroxyzine hydrochloride	TABLET, FILM COATED	ORAL	20240501	N/A	ANDA	ANDA207121	Sunrise Pharmaceutical, Inc.	HYDROXYZINE DIHYDROCHLORIDE	50 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (11534-206-01)
11534-206-03	11534-206	HUMAN PRESCRIPTION DRUG	HYDROXYZINE HYDROCHLORIDE	hydroxyzine hydrochloride	TABLET, FILM COATED	ORAL	20240501	N/A	ANDA	ANDA207121	Sunrise Pharmaceutical, Inc.	HYDROXYZINE DIHYDROCHLORIDE	50 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (11534-206-03)