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
70436-014-04	70436-014	HUMAN PRESCRIPTION DRUG	olmesartan medoxomil and amlodipine besylate and hydrochlorothiazide	olmesartan medoxomil and amlodipine besylate and hydrochlorothiazide	TABLET, FILM COATED	ORAL	20250515	N/A	ANDA	ANDA210718	Slate Run Pharmaceuticals, LLC	AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL	5 mg/1; 12.5 mg/1; 20 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (70436-014-04)
70436-014-06	70436-014	HUMAN PRESCRIPTION DRUG	olmesartan medoxomil and amlodipine besylate and hydrochlorothiazide	olmesartan medoxomil and amlodipine besylate and hydrochlorothiazide	TABLET, FILM COATED	ORAL	20250515	N/A	ANDA	ANDA210718	Slate Run Pharmaceuticals, LLC	AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL	5 mg/1; 12.5 mg/1; 20 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (70436-014-06)
70436-015-04	70436-015	HUMAN PRESCRIPTION DRUG	olmesartan medoxomil and amlodipine besylate and hydrochlorothiazide	olmesartan medoxomil and amlodipine besylate and hydrochlorothiazide	TABLET, FILM COATED	ORAL	20250515	N/A	ANDA	ANDA210718	Slate Run Pharmaceuticals, LLC	AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL	5 mg/1; 12.5 mg/1; 40 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (70436-015-04)
70436-015-06	70436-015	HUMAN PRESCRIPTION DRUG	olmesartan medoxomil and amlodipine besylate and hydrochlorothiazide	olmesartan medoxomil and amlodipine besylate and hydrochlorothiazide	TABLET, FILM COATED	ORAL	20250515	N/A	ANDA	ANDA210718	Slate Run Pharmaceuticals, LLC	AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL	5 mg/1; 12.5 mg/1; 40 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (70436-015-06)
70436-016-04	70436-016	HUMAN PRESCRIPTION DRUG	olmesartan medoxomil and amlodipine besylate and hydrochlorothiazide	olmesartan medoxomil and amlodipine besylate and hydrochlorothiazide	TABLET, FILM COATED	ORAL	20250515	N/A	ANDA	ANDA210718	Slate Run Pharmaceuticals, LLC	AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL	5 mg/1; 25 mg/1; 40 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (70436-016-04)
70436-016-06	70436-016	HUMAN PRESCRIPTION DRUG	olmesartan medoxomil and amlodipine besylate and hydrochlorothiazide	olmesartan medoxomil and amlodipine besylate and hydrochlorothiazide	TABLET, FILM COATED	ORAL	20250515	N/A	ANDA	ANDA210718	Slate Run Pharmaceuticals, LLC	AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL	5 mg/1; 25 mg/1; 40 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (70436-016-06)
70436-017-04	70436-017	HUMAN PRESCRIPTION DRUG	olmesartan medoxomil and amlodipine besylate and hydrochlorothiazide	olmesartan medoxomil and amlodipine besylate and hydrochlorothiazide	TABLET, FILM COATED	ORAL	20250515	N/A	ANDA	ANDA210718	Slate Run Pharmaceuticals, LLC	AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL	10 mg/1; 12.5 mg/1; 40 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (70436-017-04)
70436-017-06	70436-017	HUMAN PRESCRIPTION DRUG	olmesartan medoxomil and amlodipine besylate and hydrochlorothiazide	olmesartan medoxomil and amlodipine besylate and hydrochlorothiazide	TABLET, FILM COATED	ORAL	20250515	N/A	ANDA	ANDA210718	Slate Run Pharmaceuticals, LLC	AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL	10 mg/1; 12.5 mg/1; 40 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (70436-017-06)
70436-018-04	70436-018	HUMAN PRESCRIPTION DRUG	olmesartan medoxomil and amlodipine besylate and hydrochlorothiazide	olmesartan medoxomil and amlodipine besylate and hydrochlorothiazide	TABLET, FILM COATED	ORAL	20250515	N/A	ANDA	ANDA210718	Slate Run Pharmaceuticals, LLC	AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL	10 mg/1; 25 mg/1; 40 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (70436-018-04)
70436-018-06	70436-018	HUMAN PRESCRIPTION DRUG	olmesartan medoxomil and amlodipine besylate and hydrochlorothiazide	olmesartan medoxomil and amlodipine besylate and hydrochlorothiazide	TABLET, FILM COATED	ORAL	20250515	N/A	ANDA	ANDA210718	Slate Run Pharmaceuticals, LLC	AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL	10 mg/1; 25 mg/1; 40 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (70436-018-06)