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=ANDA214548"
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
76420-697-90 76420-697 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET, FILM COATED ORAL 20240302 N/A ANDA ANDA214548 Asclemed USA, Inc. AMITRIPTYLINE HYDROCHLORIDE 100 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (76420-697-90)
82868-093-90 82868-093 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET, FILM COATED ORAL 20251126 N/A ANDA ANDA214548 Northwind Health Company, LLC AMITRIPTYLINE HYDROCHLORIDE 10 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (82868-093-90)
50090-6179-0 50090-6179 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET, FILM COATED ORAL 20221020 N/A ANDA ANDA214548 A-S Medication Solutions AMITRIPTYLINE HYDROCHLORIDE 10 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (50090-6179-0)
50090-6179-1 50090-6179 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET, FILM COATED ORAL 20221020 N/A ANDA ANDA214548 A-S Medication Solutions AMITRIPTYLINE HYDROCHLORIDE 10 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (50090-6179-1)
50090-6179-6 50090-6179 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET, FILM COATED ORAL 20221020 N/A ANDA ANDA214548 A-S Medication Solutions AMITRIPTYLINE HYDROCHLORIDE 10 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (50090-6179-6)
50090-6179-7 50090-6179 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET, FILM COATED ORAL 20231221 N/A ANDA ANDA214548 A-S Medication Solutions AMITRIPTYLINE HYDROCHLORIDE 10 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (50090-6179-7)
29300-420-01 29300-420 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET, FILM COATED ORAL 20210526 N/A ANDA ANDA214548 Unichem Pharmaceuticals (USA), Inc. AMITRIPTYLINE HYDROCHLORIDE 25 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (29300-420-01)
29300-420-05 29300-420 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET, FILM COATED ORAL 20210526 N/A ANDA ANDA214548 Unichem Pharmaceuticals (USA), Inc. AMITRIPTYLINE HYDROCHLORIDE 25 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (29300-420-05)
29300-420-10 29300-420 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET, FILM COATED ORAL 20211116 N/A ANDA ANDA214548 Unichem Pharmaceuticals (USA), Inc. AMITRIPTYLINE HYDROCHLORIDE 25 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (29300-420-10)
80425-0285-1 80425-0285 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET, FILM COATED ORAL 20230322 N/A ANDA ANDA214548 Advanced Rx Pharmacy of Tennessee, LLC AMITRIPTYLINE HYDROCHLORIDE 25 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (80425-0285-1)
80425-0285-2 80425-0285 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET, FILM COATED ORAL 20230322 N/A ANDA ANDA214548 Advanced Rx Pharmacy of Tennessee, LLC AMITRIPTYLINE HYDROCHLORIDE 25 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (80425-0285-2)
80425-0285-3 80425-0285 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET, FILM COATED ORAL 20230322 N/A ANDA ANDA214548 Advanced Rx Pharmacy of Tennessee, LLC AMITRIPTYLINE HYDROCHLORIDE 25 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (80425-0285-3)
68788-8346-1 68788-8346 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET, FILM COATED ORAL 20230206 N/A ANDA ANDA214548 Preferred Pharmaceuticals Inc. AMITRIPTYLINE HYDROCHLORIDE 25 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (68788-8346-1)
68788-8346-3 68788-8346 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET, FILM COATED ORAL 20230206 N/A ANDA ANDA214548 Preferred Pharmaceuticals Inc. AMITRIPTYLINE HYDROCHLORIDE 25 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68788-8346-3)
68788-8346-6 68788-8346 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET, FILM COATED ORAL 20230206 N/A ANDA ANDA214548 Preferred Pharmaceuticals Inc. AMITRIPTYLINE HYDROCHLORIDE 25 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (68788-8346-6)
68788-8346-8 68788-8346 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET, FILM COATED ORAL 20230206 N/A ANDA ANDA214548 Preferred Pharmaceuticals Inc. AMITRIPTYLINE HYDROCHLORIDE 25 mg/1 28 TABLET, FILM COATED in 1 BOTTLE (68788-8346-8)
68788-8346-9 68788-8346 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET, FILM COATED ORAL 20230206 N/A ANDA ANDA214548 Preferred Pharmaceuticals Inc. AMITRIPTYLINE HYDROCHLORIDE 25 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68788-8346-9)
71335-9633-0 71335-9633 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET, FILM COATED ORAL 20230206 N/A ANDA ANDA214548 Bryant Ranch Prepack AMITRIPTYLINE HYDROCHLORIDE 25 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (71335-9633-0)
71335-9633-1 71335-9633 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET, FILM COATED ORAL 20230206 N/A ANDA ANDA214548 Bryant Ranch Prepack AMITRIPTYLINE HYDROCHLORIDE 25 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (71335-9633-1)
71335-9633-2 71335-9633 HUMAN PRESCRIPTION DRUG Amitriptyline Hydrochloride Amitriptyline Hydrochloride TABLET, FILM COATED ORAL 20230206 N/A ANDA ANDA214548 Bryant Ranch Prepack AMITRIPTYLINE HYDROCHLORIDE 25 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71335-9633-2)
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