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）
检索条件:" 注册申请号=ANDA209242"
符合检索条件的记录共 15 条，共 1 页，当前第 1 页 ，可点击列名称排序
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
31722-892-30 31722-892 HUMAN PRESCRIPTION DRUG Olmesartan medoxomil, amlodipine and hydrochlorothiazide Olmesartan medoxomil, amlodipine and hydrochlorothiazide TABLET, FILM COATED ORAL 20251006 N/A ANDA ANDA209242 Camber Pharmaceuticals, Inc. AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL 5 mg/1; 12.5 mg/1; 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (31722-892-30)
31722-892-32 31722-892 HUMAN PRESCRIPTION DRUG Olmesartan medoxomil, amlodipine and hydrochlorothiazide Olmesartan medoxomil, amlodipine and hydrochlorothiazide TABLET, FILM COATED ORAL 20251006 N/A ANDA ANDA209242 Camber Pharmaceuticals, Inc. AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL 5 mg/1; 12.5 mg/1; 20 mg/1 10 BLISTER PACK in 1 CARTON (31722-892-32) / 10 TABLET, FILM COATED in 1 BLISTER PACK (31722-892-31)
31722-892-90 31722-892 HUMAN PRESCRIPTION DRUG Olmesartan medoxomil, amlodipine and hydrochlorothiazide Olmesartan medoxomil, amlodipine and hydrochlorothiazide TABLET, FILM COATED ORAL 20251006 N/A ANDA ANDA209242 Camber Pharmaceuticals, Inc. AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL 5 mg/1; 12.5 mg/1; 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (31722-892-90)
31722-893-30 31722-893 HUMAN PRESCRIPTION DRUG Olmesartan medoxomil, amlodipine and hydrochlorothiazide Olmesartan medoxomil, amlodipine and hydrochlorothiazide TABLET, FILM COATED ORAL 20251006 N/A ANDA ANDA209242 Camber Pharmaceuticals, Inc. AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL 5 mg/1; 12.5 mg/1; 40 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (31722-893-30)
31722-893-32 31722-893 HUMAN PRESCRIPTION DRUG Olmesartan medoxomil, amlodipine and hydrochlorothiazide Olmesartan medoxomil, amlodipine and hydrochlorothiazide TABLET, FILM COATED ORAL 20251006 N/A ANDA ANDA209242 Camber Pharmaceuticals, Inc. AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL 5 mg/1; 12.5 mg/1; 40 mg/1 10 BLISTER PACK in 1 CARTON (31722-893-32) / 8 TABLET, FILM COATED in 1 BLISTER PACK (31722-893-31)
31722-893-90 31722-893 HUMAN PRESCRIPTION DRUG Olmesartan medoxomil, amlodipine and hydrochlorothiazide Olmesartan medoxomil, amlodipine and hydrochlorothiazide TABLET, FILM COATED ORAL 20251006 N/A ANDA ANDA209242 Camber Pharmaceuticals, Inc. AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL 5 mg/1; 12.5 mg/1; 40 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (31722-893-90)
31722-894-30 31722-894 HUMAN PRESCRIPTION DRUG Olmesartan medoxomil, amlodipine and hydrochlorothiazide Olmesartan medoxomil, amlodipine and hydrochlorothiazide TABLET, FILM COATED ORAL 20251006 N/A ANDA ANDA209242 Camber Pharmaceuticals, Inc. AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL 5 mg/1; 25 mg/1; 40 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (31722-894-30)
31722-894-32 31722-894 HUMAN PRESCRIPTION DRUG Olmesartan medoxomil, amlodipine and hydrochlorothiazide Olmesartan medoxomil, amlodipine and hydrochlorothiazide TABLET, FILM COATED ORAL 20251006 N/A ANDA ANDA209242 Camber Pharmaceuticals, Inc. AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL 5 mg/1; 25 mg/1; 40 mg/1 10 BLISTER PACK in 1 CARTON (31722-894-32) / 10 TABLET, FILM COATED in 1 BLISTER PACK (31722-894-31)
31722-894-90 31722-894 HUMAN PRESCRIPTION DRUG Olmesartan medoxomil, amlodipine and hydrochlorothiazide Olmesartan medoxomil, amlodipine and hydrochlorothiazide TABLET, FILM COATED ORAL 20251006 N/A ANDA ANDA209242 Camber Pharmaceuticals, Inc. AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL 5 mg/1; 25 mg/1; 40 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (31722-894-90)
31722-895-30 31722-895 HUMAN PRESCRIPTION DRUG Olmesartan medoxomil, amlodipine and hydrochlorothiazide Olmesartan medoxomil, amlodipine and hydrochlorothiazide TABLET, FILM COATED ORAL 20251006 N/A ANDA ANDA209242 Camber Pharmaceuticals, Inc. AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL 10 mg/1; 12.5 mg/1; 40 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (31722-895-30)
31722-895-32 31722-895 HUMAN PRESCRIPTION DRUG Olmesartan medoxomil, amlodipine and hydrochlorothiazide Olmesartan medoxomil, amlodipine and hydrochlorothiazide TABLET, FILM COATED ORAL 20251006 N/A ANDA ANDA209242 Camber Pharmaceuticals, Inc. AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL 10 mg/1; 12.5 mg/1; 40 mg/1 10 BLISTER PACK in 1 CARTON (31722-895-32) / 8 TABLET, FILM COATED in 1 BLISTER PACK (31722-895-31)
31722-895-90 31722-895 HUMAN PRESCRIPTION DRUG Olmesartan medoxomil, amlodipine and hydrochlorothiazide Olmesartan medoxomil, amlodipine and hydrochlorothiazide TABLET, FILM COATED ORAL 20251006 N/A ANDA ANDA209242 Camber Pharmaceuticals, Inc. AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL 10 mg/1; 12.5 mg/1; 40 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (31722-895-90)
31722-896-30 31722-896 HUMAN PRESCRIPTION DRUG Olmesartan medoxomil, amlodipine and hydrochlorothiazide Olmesartan medoxomil, amlodipine and hydrochlorothiazide TABLET, FILM COATED ORAL 20251006 N/A ANDA ANDA209242 Camber Pharmaceuticals, Inc. AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL 10 mg/1; 25 mg/1; 40 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (31722-896-30)
31722-896-32 31722-896 HUMAN PRESCRIPTION DRUG Olmesartan medoxomil, amlodipine and hydrochlorothiazide Olmesartan medoxomil, amlodipine and hydrochlorothiazide TABLET, FILM COATED ORAL 20251006 N/A ANDA ANDA209242 Camber Pharmaceuticals, Inc. AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL 10 mg/1; 25 mg/1; 40 mg/1 10 BLISTER PACK in 1 CARTON (31722-896-32) / 10 TABLET, FILM COATED in 1 BLISTER PACK (31722-896-31)
31722-896-90 31722-896 HUMAN PRESCRIPTION DRUG Olmesartan medoxomil, amlodipine and hydrochlorothiazide Olmesartan medoxomil, amlodipine and hydrochlorothiazide TABLET, FILM COATED ORAL 20251006 N/A ANDA ANDA209242 Camber Pharmaceuticals, Inc. AMLODIPINE BESYLATE; HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL 10 mg/1; 25 mg/1; 40 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (31722-896-90)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2026 Drugfuture->U.S. FDA National Drug Code DataBase