美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=WELLBUTRIN"
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
WELLBUTRIN 018644 001 NDA BUPROPION HYDROCHLORIDE TABLET;ORAL 50MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1985/12/30 1985/12/30 GLAXOSMITHKLINE Discontinued
WELLBUTRIN 018644 002 NDA BUPROPION HYDROCHLORIDE TABLET;ORAL 75MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1985/12/30 1985/12/30 GLAXOSMITHKLINE Discontinued
WELLBUTRIN 018644 003 NDA BUPROPION HYDROCHLORIDE TABLET;ORAL 100MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1985/12/30 1985/12/30 GLAXOSMITHKLINE Discontinued
WELLBUTRIN SR 020358 001 NDA BUPROPION HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 50MG No No 1996/10/04 1996/10/04 GLAXOSMITHKLINE Discontinued
WELLBUTRIN SR 020358 002 NDA BUPROPION HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 100MG Yes No 1996/10/04 1996/10/04 GLAXOSMITHKLINE Prescription
WELLBUTRIN SR 020358 003 NDA BUPROPION HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 150MG Yes No 1996/10/04 1996/10/04 GLAXOSMITHKLINE Prescription
WELLBUTRIN SR 020358 004 NDA BUPROPION HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 200MG Yes Yes 1996/10/04 2002/06/14 GLAXOSMITHKLINE Prescription
WELLBUTRIN XL 021515 001 NDA BUPROPION HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 150MG Yes No 2003/08/28 2003/08/28 BAUSCH Prescription
WELLBUTRIN XL 021515 002 NDA BUPROPION HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 300MG Yes Yes 2003/08/28 2003/08/28 BAUSCH Prescription
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