美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=LAMISIL"
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
LAMISIL 020192 001 NDA TERBINAFINE HYDROCHLORIDE CREAM;TOPICAL 1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** No No 1992/12/30 1992/12/30 NOVARTIS Discontinued
LAMISIL 020539 001 NDA TERBINAFINE HYDROCHLORIDE TABLET;ORAL EQ 250MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1996/05/10 1996/05/10 NOVARTIS Discontinued
LAMISIL 020749 001 NDA TERBINAFINE HYDROCHLORIDE SOLUTION;TOPICAL 1% No No 1997/10/17 1997/10/17 KARO HLTHCARE Discontinued
LAMISIL 020846 001 NDA TERBINAFINE GEL;TOPICAL 1% No No 1998/04/29 1998/04/29 KARO HLTHCARE Discontinued
LAMISIL 020980 001 NDA TERBINAFINE HYDROCHLORIDE CREAM;TOPICAL 1% Yes Yes 1999/03/09 1999/03/09 KARO HLTHCARE Over-the-counter
LAMISIL AT 021124 001 NDA TERBINAFINE HYDROCHLORIDE SOLUTION;TOPICAL 1% Yes Yes 2000/03/17 2000/03/17 KARO HLTHCARE Over-the-counter
LAMISIL AT 021124 002 NDA TERBINAFINE HYDROCHLORIDE SPRAY;TOPICAL 1% Yes Yes 2000/03/17 2000/03/17 KARO HLTHCARE Over-the-counter
LAMISIL AT 021958 001 NDA TERBINAFINE GEL;TOPICAL 1% Yes Yes 2006/07/24 2006/07/24 KARO HLTHCARE Over-the-counter
LAMISIL 022071 001 NDA TERBINAFINE HYDROCHLORIDE GRANULE;ORAL EQ 125MG BASE/PACKET Yes No 2007/09/28 2007/09/28 NOVARTIS Discontinued
LAMISIL 022071 002 NDA TERBINAFINE HYDROCHLORIDE GRANULE;ORAL EQ 187.5MG BASE/PACKET Yes No 2007/09/28 2007/09/28 NOVARTIS Discontinued
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