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=ANDA085968"
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
0781-1489-01 0781-1489 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET, FILM COATED ORAL 19771129 N/A ANDA ANDA085968 Sandoz Inc AMITRIPTYLINE HYDROCHLORIDE 75 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (0781-1489-01)
43063-836-30 43063-836 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET, FILM COATED ORAL 20180214 N/A ANDA ANDA085968 PD-Rx Pharmaceuticals, Inc. AMITRIPTYLINE HYDROCHLORIDE 50 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-836-30)
0781-1486-01 0781-1486 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET, FILM COATED ORAL 19771121 N/A ANDA ANDA085968 Sandoz Inc AMITRIPTYLINE HYDROCHLORIDE 10 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (0781-1486-01)
0781-1486-10 0781-1486 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET, FILM COATED ORAL 19771121 N/A ANDA ANDA085968 Sandoz Inc AMITRIPTYLINE HYDROCHLORIDE 10 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (0781-1486-10)
0781-1490-01 0781-1490 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET, FILM COATED ORAL 19771121 N/A ANDA ANDA085968 Sandoz Inc AMITRIPTYLINE HYDROCHLORIDE 100 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (0781-1490-01)
0781-1487-01 0781-1487 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET, FILM COATED ORAL 19771121 N/A ANDA ANDA085968 Sandoz Inc AMITRIPTYLINE HYDROCHLORIDE 25 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (0781-1487-01)
0781-1487-10 0781-1487 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET, FILM COATED ORAL 19771121 N/A ANDA ANDA085968 Sandoz Inc AMITRIPTYLINE HYDROCHLORIDE 25 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (0781-1487-10)
0781-1491-01 0781-1491 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET, FILM COATED ORAL 19771121 N/A ANDA ANDA085968 Sandoz Inc AMITRIPTYLINE HYDROCHLORIDE 150 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (0781-1491-01)
0781-1488-01 0781-1488 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET, FILM COATED ORAL 19771129 N/A ANDA ANDA085968 Sandoz Inc AMITRIPTYLINE HYDROCHLORIDE 50 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (0781-1488-01)
0781-1488-10 0781-1488 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET, FILM COATED ORAL 19771129 N/A ANDA ANDA085968 Sandoz Inc AMITRIPTYLINE HYDROCHLORIDE 50 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (0781-1488-10)
43063-822-30 43063-822 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET, FILM COATED ORAL 20180108 N/A ANDA ANDA085968 PD-Rx Pharmaceuticals, Inc. AMITRIPTYLINE HYDROCHLORIDE 25 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-822-30)
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