美国FDA药品数据库（U.S. FDA Drugs Database）
检索条件:" 药品名称=PROCAN"
符合检索条件的记录共 9 条
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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
PROCAN 085079 001 ANDA PROCAINAMIDE HYDROCHLORIDE CAPSULE;ORAL 500MG No No -- Approved Prior to Jan 1, 1982 PARKE DAVIS Discontinued
PROCAN 085804 001 ANDA PROCAINAMIDE HYDROCHLORIDE CAPSULE;ORAL 250MG No No -- Approved Prior to Jan 1, 1982 PARKE DAVIS Discontinued
PROCAN 087502 001 ANDA PROCAINAMIDE HYDROCHLORIDE CAPSULE;ORAL 375MG No No -- Approved Prior to Jan 1, 1982 PARKE DAVIS Discontinued
PROCAN SR 086468 001 ANDA PROCAINAMIDE HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 250MG Yes No 1979/12/11 Approved Prior to Jan 1, 1982 PARKE DAVIS Discontinued
PROCAN SR 088489 001 ANDA PROCAINAMIDE HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 1GM No No 1985/01/16 1985/01/16 PARKEDALE Discontinued
PROCAN SR 086065 001 ANDA PROCAINAMIDE HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 500MG Yes No 1995/09/22 Approved Prior to Jan 1, 1982 PARKEDALE Discontinued
PROCAN SR 087510 001 ANDA PROCAINAMIDE HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 750MG Yes No 1995/09/22 1982/04/01 PARKEDALE Discontinued
PROCANBID 020545 001 NDA PROCAINAMIDE HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 500MG No No 1996/01/31 1996/01/31 KING PHARMS Discontinued
PROCANBID 020545 002 NDA PROCAINAMIDE HYDROCHLORIDE TABLET, EXTENDED RELEASE;ORAL 1GM No No 1996/01/31 1996/01/31 KING PHARMS Discontinued
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