美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=METHAMPHETAMINE HYDROCHLORIDE"
商品名 申请号 产品号 申请类型 活性成分 剂型/给药途径 规格/剂量 RLD RS 申请号原始批准/暂定批准日期 产品号批准日期 申请人 市场状态
METHAMPHETAMINE HYDROCHLORIDE 086359 001 ANDA METHAMPHETAMINE HYDROCHLORIDE TABLET;ORAL 5MG No No -- Approved Prior to Jan 1, 1982 TEVA Discontinued
METHAMPHETAMINE HYDROCHLORIDE 084931 001 ANDA METHAMPHETAMINE HYDROCHLORIDE TABLET;ORAL 5MG No No 1976/01/19 Approved Prior to Jan 1, 1982 REXAR Discontinued
METHAMPHETAMINE HYDROCHLORIDE 084931 002 ANDA METHAMPHETAMINE HYDROCHLORIDE TABLET;ORAL 10MG No No 1976/01/19 Approved Prior to Jan 1, 1982 REXAR Discontinued
METHAMPHETAMINE HYDROCHLORIDE 040529 001 ANDA METHAMPHETAMINE HYDROCHLORIDE TABLET;ORAL 5MG No No 2004/02/25 2004/02/25 ABLE Discontinued
METHAMPHETAMINE HYDROCHLORIDE 091189 001 ANDA METHAMPHETAMINE HYDROCHLORIDE TABLET;ORAL 5MG No No 2010/04/21 2010/04/21 DR REDDYS LABS SA Prescription
METHAMPHETAMINE HYDROCHLORIDE 203846 001 ANDA METHAMPHETAMINE HYDROCHLORIDE TABLET;ORAL 5MG No No 2015/11/17 2015/11/17 HIKMA Prescription
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