美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=TOFRANIL"
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
TOFRANIL 011838 002 NDA IMIPRAMINE HYDROCHLORIDE INJECTABLE;INJECTION 12.5MG/ML No No 1959/10/02 Approved Prior to Jan 1, 1982 NOVARTIS Discontinued
TOFRANIL-PM 017090 001 NDA IMIPRAMINE PAMOATE CAPSULE;ORAL EQ 75MG HYDROCHLORIDE **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** Yes No 1973/03/11 Approved Prior to Jan 1, 1982 SPECGX LLC Discontinued
TOFRANIL-PM 017090 002 NDA IMIPRAMINE PAMOATE CAPSULE;ORAL EQ 150MG HYDROCHLORIDE **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** Yes No 1973/03/11 Approved Prior to Jan 1, 1982 SPECGX LLC Discontinued
TOFRANIL-PM 017090 003 NDA IMIPRAMINE PAMOATE CAPSULE;ORAL EQ 125MG HYDROCHLORIDE **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** Yes No 1973/03/11 Approved Prior to Jan 1, 1982 SPECGX LLC Discontinued
TOFRANIL-PM 017090 004 NDA IMIPRAMINE PAMOATE CAPSULE;ORAL EQ 100MG HYDROCHLORIDE **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** Yes No 1973/03/11 Approved Prior to Jan 1, 1982 SPECGX LLC Discontinued
TOFRANIL 087844 001 ANDA IMIPRAMINE HYDROCHLORIDE TABLET;ORAL 10MG No 1984/05/22 MALLINCKRODT INC Prescription
TOFRANIL 087845 001 ANDA IMIPRAMINE HYDROCHLORIDE TABLET;ORAL 25MG No 1984/05/22 MALLINCKRODT INC Prescription
TOFRANIL 087846 001 ANDA IMIPRAMINE HYDROCHLORIDE TABLET;ORAL 50MG No Yes 1984/05/22 1984/05/22 SPECGX LLC Prescription
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