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=ANDA203281"
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
71335-0999-3 71335-0999 HUMAN PRESCRIPTION DRUG olmesartan medoxomil olmesartan medoxomil TABLET, FILM COATED ORAL 20180823 N/A ANDA ANDA203281 Bryant Ranch Prepack OLMESARTAN MEDOXOMIL 40 mg/1 28 TABLET, FILM COATED in 1 BOTTLE (71335-0999-3)
71335-0999-1 71335-0999 HUMAN PRESCRIPTION DRUG olmesartan medoxomil olmesartan medoxomil TABLET, FILM COATED ORAL 20180823 N/A ANDA ANDA203281 Bryant Ranch Prepack OLMESARTAN MEDOXOMIL 40 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71335-0999-1)
71335-0999-2 71335-0999 HUMAN PRESCRIPTION DRUG olmesartan medoxomil olmesartan medoxomil TABLET, FILM COATED ORAL 20180823 N/A ANDA ANDA203281 Bryant Ranch Prepack OLMESARTAN MEDOXOMIL 40 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71335-0999-2)
68462-436-10 68462-436 HUMAN PRESCRIPTION DRUG Olmesartan Medoxomil Olmesartan Medoxomil TABLET, FILM COATED ORAL 20170525 N/A ANDA ANDA203281 Glenmark Pharmaceuticals Inc., USA OLMESARTAN MEDOXOMIL 5 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (68462-436-10)
68462-436-30 68462-436 HUMAN PRESCRIPTION DRUG Olmesartan Medoxomil Olmesartan Medoxomil TABLET, FILM COATED ORAL 20170525 N/A ANDA ANDA203281 Glenmark Pharmaceuticals Inc., USA OLMESARTAN MEDOXOMIL 5 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68462-436-30)
68462-436-90 68462-436 HUMAN PRESCRIPTION DRUG Olmesartan Medoxomil Olmesartan Medoxomil TABLET, FILM COATED ORAL 20170525 N/A ANDA ANDA203281 Glenmark Pharmaceuticals Inc., USA OLMESARTAN MEDOXOMIL 5 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68462-436-90)
68462-437-10 68462-437 HUMAN PRESCRIPTION DRUG Olmesartan Medoxomil Olmesartan Medoxomil TABLET, FILM COATED ORAL 20170525 N/A ANDA ANDA203281 Glenmark Pharmaceuticals Inc., USA OLMESARTAN MEDOXOMIL 20 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (68462-437-10)
68462-437-11 68462-437 HUMAN PRESCRIPTION DRUG Olmesartan Medoxomil Olmesartan Medoxomil TABLET, FILM COATED ORAL 20170525 N/A ANDA ANDA203281 Glenmark Pharmaceuticals Inc., USA OLMESARTAN MEDOXOMIL 20 mg/1 10 BLISTER PACK in 1 CARTON (68462-437-11) / 10 TABLET, FILM COATED in 1 BLISTER PACK
68462-437-30 68462-437 HUMAN PRESCRIPTION DRUG Olmesartan Medoxomil Olmesartan Medoxomil TABLET, FILM COATED ORAL 20170525 N/A ANDA ANDA203281 Glenmark Pharmaceuticals Inc., USA OLMESARTAN MEDOXOMIL 20 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68462-437-30)
68462-437-90 68462-437 HUMAN PRESCRIPTION DRUG Olmesartan Medoxomil Olmesartan Medoxomil TABLET, FILM COATED ORAL 20170525 N/A ANDA ANDA203281 Glenmark Pharmaceuticals Inc., USA OLMESARTAN MEDOXOMIL 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68462-437-90)
68462-438-10 68462-438 HUMAN PRESCRIPTION DRUG Olmesartan Medoxomil Olmesartan Medoxomil TABLET, FILM COATED ORAL 20170525 N/A ANDA ANDA203281 Glenmark Pharmaceuticals Inc., USA OLMESARTAN MEDOXOMIL 40 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (68462-438-10)
68462-438-11 68462-438 HUMAN PRESCRIPTION DRUG Olmesartan Medoxomil Olmesartan Medoxomil TABLET, FILM COATED ORAL 20170525 N/A ANDA ANDA203281 Glenmark Pharmaceuticals Inc., USA OLMESARTAN MEDOXOMIL 40 mg/1 10 BLISTER PACK in 1 CARTON (68462-438-11) / 10 TABLET, FILM COATED in 1 BLISTER PACK
68462-438-30 68462-438 HUMAN PRESCRIPTION DRUG Olmesartan Medoxomil Olmesartan Medoxomil TABLET, FILM COATED ORAL 20170525 N/A ANDA ANDA203281 Glenmark Pharmaceuticals Inc., USA OLMESARTAN MEDOXOMIL 40 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68462-438-30)
68462-438-90 68462-438 HUMAN PRESCRIPTION DRUG Olmesartan Medoxomil Olmesartan Medoxomil TABLET, FILM COATED ORAL 20170525 N/A ANDA ANDA203281 Glenmark Pharmaceuticals Inc., USA OLMESARTAN MEDOXOMIL 40 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68462-438-90)
50090-6686-0 50090-6686 HUMAN PRESCRIPTION DRUG Olmesartan Medoxomil Olmesartan Medoxomil TABLET, FILM COATED ORAL 20230915 N/A ANDA ANDA203281 A-S Medication Solutions OLMESARTAN MEDOXOMIL 20 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (50090-6686-0)
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