美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=LIBRIUM"
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
LIBRIUM 012249 001 NDA CHLORDIAZEPOXIDE HYDROCHLORIDE CAPSULE;ORAL 10MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1960/02/24 Approved Prior to Jan 1, 1982 VALEANT PHARM INTL Discontinued
LIBRIUM 012249 002 NDA CHLORDIAZEPOXIDE HYDROCHLORIDE CAPSULE;ORAL 5MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1960/02/24 Approved Prior to Jan 1, 1982 VALEANT PHARM INTL Discontinued
LIBRIUM 012249 003 NDA CHLORDIAZEPOXIDE HYDROCHLORIDE CAPSULE;ORAL 25MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1960/02/24 Approved Prior to Jan 1, 1982 VALEANT PHARM INTL Discontinued
LIBRIUM 012301 001 NDA CHLORDIAZEPOXIDE HYDROCHLORIDE INJECTABLE;INJECTION 100MG/AMP No No 1961/07/21 Approved Prior to Jan 1, 1982 BAUSCH Discontinued
LIBRIUM 085461 001 ANDA CHLORDIAZEPOXIDE HYDROCHLORIDE CAPSULE;ORAL 5MG Yes No 1977/09/21 Approved Prior to Jan 1, 1982 VALEANT PHARM INTL Prescription
LIBRIUM 085472 001 ANDA CHLORDIAZEPOXIDE HYDROCHLORIDE CAPSULE;ORAL 10MG Yes No 1977/09/21 Approved Prior to Jan 1, 1982 VALEANT PHARM INTL Prescription
LIBRIUM 085475 001 ANDA CHLORDIAZEPOXIDE HYDROCHLORIDE CAPSULE;ORAL 25MG Yes No 1977/09/21 Approved Prior to Jan 1, 1982 BAUSCH Prescription
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