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=ANDA208537"
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
76282-550-01 76282-550 HUMAN PRESCRIPTION DRUG TICAGRELOR TICAGRELOR TABLET, FILM COATED ORAL 20250507 N/A ANDA ANDA208537 Exelan Pharmaceuticals, Inc TICAGRELOR 90 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (76282-550-01)
76282-550-05 76282-550 HUMAN PRESCRIPTION DRUG TICAGRELOR TICAGRELOR TABLET, FILM COATED ORAL 20250507 N/A ANDA ANDA208537 Exelan Pharmaceuticals, Inc TICAGRELOR 90 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (76282-550-05)
76282-550-60 76282-550 HUMAN PRESCRIPTION DRUG TICAGRELOR TICAGRELOR TABLET, FILM COATED ORAL 20250507 N/A ANDA ANDA208537 Exelan Pharmaceuticals, Inc TICAGRELOR 90 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (76282-550-60)
76282-584-01 76282-584 HUMAN PRESCRIPTION DRUG TICAGRELOR TICAGRELOR TABLET, FILM COATED ORAL 20251029 N/A ANDA ANDA208537 Exelan Pharmaceuticals, Inc TICAGRELOR 60 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (76282-584-01)
76282-584-05 76282-584 HUMAN PRESCRIPTION DRUG TICAGRELOR TICAGRELOR TABLET, FILM COATED ORAL 20251029 N/A ANDA ANDA208537 Exelan Pharmaceuticals, Inc TICAGRELOR 60 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (76282-584-05)
76282-584-60 76282-584 HUMAN PRESCRIPTION DRUG TICAGRELOR TICAGRELOR TABLET, FILM COATED ORAL 20251029 N/A ANDA ANDA208537 Exelan Pharmaceuticals, Inc TICAGRELOR 60 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (76282-584-60)
71610-914-41 71610-914 HUMAN PRESCRIPTION DRUG TICAGRELOR TICAGRELOR TABLET, FILM COATED ORAL 20250613 N/A ANDA ANDA208537 Aphena Pharma Solutions - Tennessee, LLC TICAGRELOR 90 mg/1 5400 TABLET, FILM COATED in 1 BOTTLE (71610-914-41)
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