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
33342-244-10	33342-244	HUMAN PRESCRIPTION DRUG	Olmesartan medoxomil Amlodipine and Hydrochlorothiazide	Olmesartan medoxomil Amlodipine and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20250718	N/A	ANDA	ANDA207088	Macleods Pharmaceuticals Limited	AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL	5 mg/1; 12.5 mg/1; 40 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (33342-244-10)
33342-245-07	33342-245	HUMAN PRESCRIPTION DRUG	Olmesartan medoxomil Amlodipine and Hydrochlorothiazide	Olmesartan medoxomil Amlodipine and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20250718	N/A	ANDA	ANDA207088	Macleods Pharmaceuticals Limited	AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL	5 mg/1; 25 mg/1; 40 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (33342-245-07)
33342-245-10	33342-245	HUMAN PRESCRIPTION DRUG	Olmesartan medoxomil Amlodipine and Hydrochlorothiazide	Olmesartan medoxomil Amlodipine and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20250718	N/A	ANDA	ANDA207088	Macleods Pharmaceuticals Limited	AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL	5 mg/1; 25 mg/1; 40 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (33342-245-10)
33342-246-07	33342-246	HUMAN PRESCRIPTION DRUG	Olmesartan medoxomil Amlodipine and Hydrochlorothiazide	Olmesartan medoxomil Amlodipine and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20250718	N/A	ANDA	ANDA207088	Macleods Pharmaceuticals Limited	AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL	10 mg/1; 12.5 mg/1; 40 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (33342-246-07)
33342-246-10	33342-246	HUMAN PRESCRIPTION DRUG	Olmesartan medoxomil Amlodipine and Hydrochlorothiazide	Olmesartan medoxomil Amlodipine and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20250718	N/A	ANDA	ANDA207088	Macleods Pharmaceuticals Limited	AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL	10 mg/1; 12.5 mg/1; 40 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (33342-246-10)
33342-247-07	33342-247	HUMAN PRESCRIPTION DRUG	Olmesartan medoxomil Amlodipine and Hydrochlorothiazide	Olmesartan medoxomil Amlodipine and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20250718	N/A	ANDA	ANDA207088	Macleods Pharmaceuticals Limited	AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL	10 mg/1; 25 mg/1; 40 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (33342-247-07)
33342-247-10	33342-247	HUMAN PRESCRIPTION DRUG	Olmesartan medoxomil Amlodipine and Hydrochlorothiazide	Olmesartan medoxomil Amlodipine and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20250718	N/A	ANDA	ANDA207088	Macleods Pharmaceuticals Limited	AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL	10 mg/1; 25 mg/1; 40 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (33342-247-10)
33342-244-07	33342-244	HUMAN PRESCRIPTION DRUG	Olmesartan medoxomil Amlodipine and Hydrochlorothiazide	Olmesartan medoxomil Amlodipine and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20250718	N/A	ANDA	ANDA207088	Macleods Pharmaceuticals Limited	AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL	5 mg/1; 12.5 mg/1; 40 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (33342-244-07)
33342-243-10	33342-243	HUMAN PRESCRIPTION DRUG	Olmesartan medoxomil Amlodipine and Hydrochlorothiazide	Olmesartan medoxomil Amlodipine and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20250718	N/A	ANDA	ANDA207088	Macleods Pharmaceuticals Limited	AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL	5 mg/1; 12.5 mg/1; 20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (33342-243-10)
33342-243-07	33342-243	HUMAN PRESCRIPTION DRUG	Olmesartan medoxomil Amlodipine and Hydrochlorothiazide	Olmesartan medoxomil Amlodipine and Hydrochlorothiazide	TABLET, FILM COATED	ORAL	20250718	N/A	ANDA	ANDA207088	Macleods Pharmaceuticals Limited	AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL	5 mg/1; 12.5 mg/1; 20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (33342-243-07)