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"
符合检索条件的记录共 115 条，共 6 页，当前第 5 页 ，可点击列名称排序
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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
68788-8121-4 68788-8121 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20220105 N/A ANDA ANDA208708 Preferred Pharmaceuticals Inc. TRAMADOL HYDROCHLORIDE 50 mg/1 40 TABLET, COATED in 1 BOTTLE (68788-8121-4)
68788-8121-5 68788-8121 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20220105 N/A ANDA ANDA208708 Preferred Pharmaceuticals Inc. TRAMADOL HYDROCHLORIDE 50 mg/1 15 TABLET, COATED in 1 BOTTLE (68788-8121-5)
67296-1834-1 67296-1834 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20210422 N/A ANDA ANDA208708 RedPharm Drug Inc TRAMADOL HYDROCHLORIDE 50 mg/1 10 TABLET, COATED in 1 BOTTLE (67296-1834-1)
67296-1834-2 67296-1834 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20210422 N/A ANDA ANDA208708 RedPharm Drug Inc TRAMADOL HYDROCHLORIDE 50 mg/1 20 TABLET, COATED in 1 BOTTLE (67296-1834-2)
67296-1834-3 67296-1834 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20210422 N/A ANDA ANDA208708 RedPharm Drug Inc TRAMADOL HYDROCHLORIDE 50 mg/1 30 TABLET, COATED in 1 BOTTLE (67296-1834-3)
67296-1834-4 67296-1834 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20210422 N/A ANDA ANDA208708 RedPharm Drug Inc TRAMADOL HYDROCHLORIDE 50 mg/1 40 TABLET, COATED in 1 BOTTLE (67296-1834-4)
67296-1834-6 67296-1834 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20210422 N/A ANDA ANDA208708 RedPharm Drug Inc TRAMADOL HYDROCHLORIDE 50 mg/1 6 TABLET, COATED in 1 BOTTLE (67296-1834-6)
67296-1834-7 67296-1834 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20210422 N/A ANDA ANDA208708 RedPharm Drug Inc TRAMADOL HYDROCHLORIDE 50 mg/1 15 TABLET, COATED in 1 BOTTLE (67296-1834-7)
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)
76420-733-02 76420-733 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20250814 N/A ANDA ANDA208708 Asclemed USA, Inc. TRAMADOL HYDROCHLORIDE 50 mg/1 2 TABLET, COATED in 1 BOTTLE (76420-733-02)
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)
76420-733-10 76420-733 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20250814 N/A ANDA ANDA208708 Asclemed USA, Inc. TRAMADOL HYDROCHLORIDE 50 mg/1 1 TABLET, COATED in 1 BOTTLE (76420-733-10)
76420-733-12 76420-733 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, COATED ORAL 20250714 N/A ANDA ANDA208708 Asclemed USA, Inc. TRAMADOL HYDROCHLORIDE 50 mg/1 120 TABLET, COATED in 1 BOTTLE (76420-733-12)
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