美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=RITALIN"
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
RITALIN 010187 003 NDA METHYLPHENIDATE HYDROCHLORIDE TABLET;ORAL 5MG Yes No 1955/12/05 Approved Prior to Jan 1, 1982 NOVARTIS Prescription
RITALIN 010187 006 NDA METHYLPHENIDATE HYDROCHLORIDE TABLET;ORAL 10MG Yes No 1955/12/05 Approved Prior to Jan 1, 1982 NOVARTIS Prescription
RITALIN 010187 010 NDA METHYLPHENIDATE HYDROCHLORIDE TABLET;ORAL 20MG Yes Yes 1955/12/05 Approved Prior to Jan 1, 1982 NOVARTIS Prescription
RITALIN-SR 018029 001 NDA METHYLPHENIDATE HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 20MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** Yes No 1982/03/30 1982/03/30 NOVARTIS Discontinued
RITALIN LA 021284 001 NDA METHYLPHENIDATE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL 20MG Yes No 2002/06/05 2002/06/05 NOVARTIS Prescription
RITALIN LA 021284 002 NDA METHYLPHENIDATE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL 30MG Yes No 2002/06/05 2002/06/05 NOVARTIS Prescription
RITALIN LA 021284 003 NDA METHYLPHENIDATE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL 40MG Yes No 2002/06/05 2002/06/05 NOVARTIS Prescription
RITALIN LA 021284 004 NDA METHYLPHENIDATE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL 10MG Yes No 2002/06/05 2004/04/10 NOVARTIS Prescription
RITALIN LA 021284 005 NDA METHYLPHENIDATE HYDROCHLORIDE CAPSULE, EXTENDED RELEASE;ORAL 60MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** Yes No 2002/06/05 2014/10/27 NOVARTIS Discontinued
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