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=ANDA211825"
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
68788-4040-4 68788-4040 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, FILM COATED ORAL 20251013 N/A ANDA ANDA211825 Preferred Pharmaceuticals Inc. TRAMADOL HYDROCHLORIDE 50 mg/1 40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-4040-4)
68788-4040-5 68788-4040 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, FILM COATED ORAL 20251013 N/A ANDA ANDA211825 Preferred Pharmaceuticals Inc. TRAMADOL HYDROCHLORIDE 50 mg/1 15 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-4040-5)
68788-4040-6 68788-4040 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, FILM COATED ORAL 20251013 N/A ANDA ANDA211825 Preferred Pharmaceuticals Inc. TRAMADOL HYDROCHLORIDE 50 mg/1 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-4040-6)
68788-4040-7 68788-4040 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, FILM COATED ORAL 20251013 N/A ANDA ANDA211825 Preferred Pharmaceuticals Inc. TRAMADOL HYDROCHLORIDE 50 mg/1 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-4040-7)
68788-4040-8 68788-4040 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, FILM COATED ORAL 20251013 N/A ANDA ANDA211825 Preferred Pharmaceuticals Inc. TRAMADOL HYDROCHLORIDE 50 mg/1 120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-4040-8)
68788-4040-9 68788-4040 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, FILM COATED ORAL 20251013 N/A ANDA ANDA211825 Preferred Pharmaceuticals Inc. TRAMADOL HYDROCHLORIDE 50 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-4040-9)
87063-117-01 87063-117 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, FILM COATED ORAL 20260216 N/A ANDA ANDA211825 Asclemed USA, Inc. TRAMADOL HYDROCHLORIDE 50 mg/1 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (87063-117-01)
87063-117-05 87063-117 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, FILM COATED ORAL 20260216 N/A ANDA ANDA211825 Asclemed USA, Inc. TRAMADOL HYDROCHLORIDE 50 mg/1 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (87063-117-05)
87063-117-10 87063-117 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, FILM COATED ORAL 20260216 N/A ANDA ANDA211825 Asclemed USA, Inc. TRAMADOL HYDROCHLORIDE 50 mg/1 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (87063-117-10)
87063-117-20 87063-117 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, FILM COATED ORAL 20260216 N/A ANDA ANDA211825 Asclemed USA, Inc. TRAMADOL HYDROCHLORIDE 50 mg/1 20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (87063-117-20)
87063-117-30 87063-117 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, FILM COATED ORAL 20260216 N/A ANDA ANDA211825 Asclemed USA, Inc. TRAMADOL HYDROCHLORIDE 50 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (87063-117-30)
87063-117-50 87063-117 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, FILM COATED ORAL 20260216 N/A ANDA ANDA211825 Asclemed USA, Inc. TRAMADOL HYDROCHLORIDE 50 mg/1 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (87063-117-50)
87063-117-60 87063-117 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, FILM COATED ORAL 20260216 N/A ANDA ANDA211825 Asclemed USA, Inc. TRAMADOL HYDROCHLORIDE 50 mg/1 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (87063-117-60)
87063-117-90 87063-117 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, FILM COATED ORAL 20260216 N/A ANDA ANDA211825 Asclemed USA, Inc. TRAMADOL HYDROCHLORIDE 50 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (87063-117-90)
50090-5789-0 50090-5789 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, FILM COATED ORAL 20211008 N/A ANDA ANDA211825 A-S Medication Solutions TRAMADOL HYDROCHLORIDE 50 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (50090-5789-0)
50090-5789-1 50090-5789 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, FILM COATED ORAL 20211008 N/A ANDA ANDA211825 A-S Medication Solutions TRAMADOL HYDROCHLORIDE 50 mg/1 20 TABLET, FILM COATED in 1 BOTTLE (50090-5789-1)
50090-5789-2 50090-5789 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, FILM COATED ORAL 20211008 N/A ANDA ANDA211825 A-S Medication Solutions TRAMADOL HYDROCHLORIDE 50 mg/1 50 TABLET, FILM COATED in 1 BOTTLE (50090-5789-2)
50090-5789-4 50090-5789 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, FILM COATED ORAL 20211008 N/A ANDA ANDA211825 A-S Medication Solutions TRAMADOL HYDROCHLORIDE 50 mg/1 15 TABLET, FILM COATED in 1 BOTTLE (50090-5789-4)
50090-5789-5 50090-5789 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, FILM COATED ORAL 20211008 N/A ANDA ANDA211825 A-S Medication Solutions TRAMADOL HYDROCHLORIDE 50 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (50090-5789-5)
50090-5789-9 50090-5789 HUMAN PRESCRIPTION DRUG Tramadol Hydrochloride Tramadol Hydrochloride TABLET, FILM COATED ORAL 20211008 N/A ANDA ANDA211825 A-S Medication Solutions TRAMADOL HYDROCHLORIDE 50 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (50090-5789-9)
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