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=ANDA208708"
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
80425-0276-8 80425-0276 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20230331 N/A ANDA ANDA208708 Advanced Rx Pharmacy of Tennessee, LLC TRAMADOL HYDROCHLORIDE 50 mg/1 240 TABLET, COATED in 1 BOTTLE (80425-0276-8)
82804-142-15 82804-142 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20241021 N/A ANDA ANDA208708 Proficient Rx LP TRAMADOL HYDROCHLORIDE 50 mg/1 15 TABLET, COATED in 1 BOTTLE (82804-142-15)
82804-142-20 82804-142 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20240919 N/A ANDA ANDA208708 Proficient Rx LP TRAMADOL HYDROCHLORIDE 50 mg/1 20 TABLET, COATED in 1 BOTTLE (82804-142-20)
82804-142-30 82804-142 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20240919 N/A ANDA ANDA208708 Proficient Rx LP TRAMADOL HYDROCHLORIDE 50 mg/1 30 TABLET, COATED in 1 BOTTLE (82804-142-30)
82804-142-60 82804-142 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20240919 N/A ANDA ANDA208708 Proficient Rx LP TRAMADOL HYDROCHLORIDE 50 mg/1 60 TABLET, COATED in 1 BOTTLE (82804-142-60)
82804-142-90 82804-142 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20240919 N/A ANDA ANDA208708 Proficient Rx LP TRAMADOL HYDROCHLORIDE 50 mg/1 90 TABLET, COATED in 1 BOTTLE (82804-142-90)
67296-1917-7 67296-1917 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20200224 N/A ANDA ANDA208708 RedPharm Drug TRAMADOL HYDROCHLORIDE 100 mg/1 15 TABLET, COATED in 1 BOTTLE (67296-1917-7)
76420-732-00 76420-732 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20240522 N/A ANDA ANDA208708 Asclemed USA, Inc. TRAMADOL HYDROCHLORIDE 25 mg/1 1000 TABLET, COATED in 1 BOTTLE (76420-732-00)
76420-732-01 76420-732 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20240522 N/A ANDA ANDA208708 Asclemed USA, Inc. TRAMADOL HYDROCHLORIDE 25 mg/1 100 TABLET, COATED in 1 BOTTLE (76420-732-01)
76420-732-05 76420-732 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20240522 N/A ANDA ANDA208708 Asclemed USA, Inc. TRAMADOL HYDROCHLORIDE 25 mg/1 500 TABLET, COATED in 1 BOTTLE (76420-732-05)
76420-732-30 76420-732 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20240522 N/A ANDA ANDA208708 Asclemed USA, Inc. TRAMADOL HYDROCHLORIDE 25 mg/1 30 TABLET, COATED in 1 BOTTLE (76420-732-30)
76420-732-60 76420-732 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20240522 N/A ANDA ANDA208708 Asclemed USA, Inc. TRAMADOL HYDROCHLORIDE 25 mg/1 60 TABLET, COATED in 1 BOTTLE (76420-732-60)
76420-732-90 76420-732 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20240522 N/A ANDA ANDA208708 Asclemed USA, Inc. TRAMADOL HYDROCHLORIDE 25 mg/1 90 TABLET, COATED in 1 BOTTLE (76420-732-90)
76420-733-00 76420-733 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20240522 N/A ANDA ANDA208708 Asclemed USA, Inc. TRAMADOL HYDROCHLORIDE 50 mg/1 1000 TABLET, COATED in 1 BOTTLE (76420-733-00)
76420-733-01 76420-733 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20240522 N/A ANDA ANDA208708 Asclemed USA, Inc. TRAMADOL HYDROCHLORIDE 50 mg/1 100 TABLET, COATED in 1 BOTTLE (76420-733-01)
76420-733-05 76420-733 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20240522 N/A ANDA ANDA208708 Asclemed USA, Inc. TRAMADOL HYDROCHLORIDE 50 mg/1 500 TABLET, COATED in 1 BOTTLE (76420-733-05)
76420-733-30 76420-733 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20240522 N/A ANDA ANDA208708 Asclemed USA, Inc. TRAMADOL HYDROCHLORIDE 50 mg/1 30 TABLET, COATED in 1 BOTTLE (76420-733-30)
76420-733-60 76420-733 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20240522 N/A ANDA ANDA208708 Asclemed USA, Inc. TRAMADOL HYDROCHLORIDE 50 mg/1 60 TABLET, COATED in 1 BOTTLE (76420-733-60)
76420-733-90 76420-733 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20240522 N/A ANDA ANDA208708 Asclemed USA, Inc. TRAMADOL HYDROCHLORIDE 50 mg/1 90 TABLET, COATED in 1 BOTTLE (76420-733-90)
76420-734-00 76420-734 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20240522 N/A ANDA ANDA208708 Asclemed USA, Inc. TRAMADOL HYDROCHLORIDE 100 mg/1 1000 TABLET, COATED in 1 BOTTLE (76420-734-00)
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