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=ANDA204165"
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
68071-5277-9 68071-5277 HUMAN PRESCRIPTION DRUG Clopidogrel bisulfate Clopidogrel bisulfate TABLET, FILM COATED ORAL 20200610 N/A ANDA ANDA204165 NuCare Pharmaceuticals,Inc. CLOPIDOGREL BISULFATE 75 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68071-5277-9)
50228-124-05 50228-124 HUMAN PRESCRIPTION DRUG Clopidogrel bisulfate Clopidogrel bisulfate TABLET, FILM COATED ORAL 20150915 N/A ANDA ANDA204165 ScieGen Pharmaceuticals Inc CLOPIDOGREL BISULFATE 75 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (50228-124-05)
50228-124-10 50228-124 HUMAN PRESCRIPTION DRUG Clopidogrel bisulfate Clopidogrel bisulfate TABLET, FILM COATED ORAL 20150915 N/A ANDA ANDA204165 ScieGen Pharmaceuticals Inc CLOPIDOGREL BISULFATE 75 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (50228-124-10)
50228-124-30 50228-124 HUMAN PRESCRIPTION DRUG Clopidogrel bisulfate Clopidogrel bisulfate TABLET, FILM COATED ORAL 20150915 N/A ANDA ANDA204165 ScieGen Pharmaceuticals Inc CLOPIDOGREL BISULFATE 75 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (50228-124-30)
50228-124-90 50228-124 HUMAN PRESCRIPTION DRUG Clopidogrel bisulfate Clopidogrel bisulfate TABLET, FILM COATED ORAL 20150915 N/A ANDA ANDA204165 ScieGen Pharmaceuticals Inc CLOPIDOGREL BISULFATE 75 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (50228-124-90)
70518-4110-0 70518-4110 HUMAN PRESCRIPTION DRUG Clopidogrel bisulfate Clopidogrel bisulfate TABLET, FILM COATED ORAL 20240624 N/A ANDA ANDA204165 REMEDYREPACK INC. CLOPIDOGREL BISULFATE 75 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4110-0)
70518-4110-1 70518-4110 HUMAN PRESCRIPTION DRUG Clopidogrel bisulfate Clopidogrel bisulfate TABLET, FILM COATED ORAL 20240711 N/A ANDA ANDA204165 REMEDYREPACK INC. CLOPIDOGREL BISULFATE 75 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4110-1)
70518-4110-2 70518-4110 HUMAN PRESCRIPTION DRUG Clopidogrel bisulfate Clopidogrel bisulfate TABLET, FILM COATED ORAL 20241217 N/A ANDA ANDA204165 REMEDYREPACK INC. CLOPIDOGREL BISULFATE 75 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4110-2)
50228-121-05 50228-121 HUMAN PRESCRIPTION DRUG Clopidogrel bisulfate Clopidogrel bisulfate TABLET, FILM COATED ORAL 20150915 N/A ANDA ANDA204165 ScieGen Pharmaceuticals Inc CLOPIDOGREL BISULFATE 300 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (50228-121-05)
50228-121-30 50228-121 HUMAN PRESCRIPTION DRUG Clopidogrel bisulfate Clopidogrel bisulfate TABLET, FILM COATED ORAL 20150915 N/A ANDA ANDA204165 ScieGen Pharmaceuticals Inc CLOPIDOGREL BISULFATE 300 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (50228-121-30)
50228-121-90 50228-121 HUMAN PRESCRIPTION DRUG Clopidogrel bisulfate Clopidogrel bisulfate TABLET, FILM COATED ORAL 20150915 N/A ANDA ANDA204165 ScieGen Pharmaceuticals Inc CLOPIDOGREL BISULFATE 300 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (50228-121-90)
0615-8625-05 0615-8625 HUMAN PRESCRIPTION DRUG Clopidogrel bisulfate Clopidogrel bisulfate TABLET, FILM COATED ORAL 20260217 N/A ANDA ANDA204165 NCS HealthCare of KY, LLC dba Vangard Labs CLOPIDOGREL BISULFATE 75 mg/1 15 TABLET, FILM COATED in 1 BLISTER PACK (0615-8625-05)
0615-8625-07 0615-8625 HUMAN PRESCRIPTION DRUG Clopidogrel bisulfate Clopidogrel bisulfate TABLET, FILM COATED ORAL 20260217 N/A ANDA ANDA204165 NCS HealthCare of KY, LLC dba Vangard Labs CLOPIDOGREL BISULFATE 75 mg/1 7 TABLET, FILM COATED in 1 BLISTER PACK (0615-8625-07)
0615-8625-30 0615-8625 HUMAN PRESCRIPTION DRUG Clopidogrel bisulfate Clopidogrel bisulfate TABLET, FILM COATED ORAL 20260213 N/A ANDA ANDA204165 NCS HealthCare of KY, LLC dba Vangard Labs CLOPIDOGREL BISULFATE 75 mg/1 6 BLISTER PACK in 1 BOX, UNIT-DOSE (0615-8625-30) / 5 TABLET, FILM COATED in 1 BLISTER PACK
0615-8625-39 0615-8625 HUMAN PRESCRIPTION DRUG Clopidogrel bisulfate Clopidogrel bisulfate TABLET, FILM COATED ORAL 20260217 N/A ANDA ANDA204165 NCS HealthCare of KY, LLC dba Vangard Labs CLOPIDOGREL BISULFATE 75 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8625-39)
82804-986-00 82804-986 HUMAN PRESCRIPTION DRUG Clopidogrel Clopidogrel Bisulfate TABLET, FILM COATED ORAL 20240521 N/A ANDA ANDA204165 Proficient Rx LP CLOPIDOGREL BISULFATE 300 mg/1 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (82804-986-00)
70518-4110-3 70518-4110 HUMAN PRESCRIPTION DRUG Clopidogrel bisulfate Clopidogrel bisulfate TABLET, FILM COATED ORAL 20250218 N/A ANDA ANDA204165 REMEDYREPACK INC. CLOPIDOGREL BISULFATE 75 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4110-3)
70518-4110-4 70518-4110 HUMAN PRESCRIPTION DRUG Clopidogrel bisulfate Clopidogrel bisulfate TABLET, FILM COATED ORAL 20250324 N/A ANDA ANDA204165 REMEDYREPACK INC. CLOPIDOGREL BISULFATE 75 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4110-4)
42543-713-01 42543-713 HUMAN PRESCRIPTION DRUG Clopidogrel clopidogrel TABLET ORAL 20141101 N/A ANDA ANDA204165 Vensun Pharmaceuticals, Inc. CLOPIDOGREL BISULFATE 75 mg/1 100 TABLET in 1 BOTTLE (42543-713-01)
42543-713-05 42543-713 HUMAN PRESCRIPTION DRUG Clopidogrel clopidogrel TABLET ORAL 20141101 N/A ANDA ANDA204165 Vensun Pharmaceuticals, Inc. CLOPIDOGREL BISULFATE 75 mg/1 500 TABLET in 1 BOTTLE (42543-713-05)
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