美国FDA药品数据库（U.S. FDA Drugs Database）
检索条件:" 药品名称=IMODIUM"
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
IMODIUM 017690 001 NDA LOPERAMIDE HYDROCHLORIDE CAPSULE;ORAL 2MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** No No 1976/12/28 Approved Prior to Jan 1, 1982 J AND J CONSUMER INC Discontinued
IMODIUM 017694 001 NDA LOPERAMIDE HYDROCHLORIDE CAPSULE;ORAL 2MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No 1976/12/28 Approved Prior to Jan 1, 1982 J AND J CONSUMER INC Discontinued
IMODIUM 019037 001 NDA LOPERAMIDE HYDROCHLORIDE SOLUTION;ORAL 1MG/5ML No No 1984/07/31 1984/07/31 JANSSEN PHARMS Discontinued
IMODIUM A-D 019487 001 NDA LOPERAMIDE HYDROCHLORIDE SOLUTION;ORAL 1MG/5ML Yes Yes 1988/03/01 1988/03/01 J AND J CONSUMER INC Over-the-counter
IMODIUM A-D 019487 002 NDA LOPERAMIDE HYDROCHLORIDE SUSPENSION;ORAL 1MG/7.5ML Yes Yes 1988/03/01 2004/07/08 J AND J CONSUMER INC Over-the-counter
IMODIUM A-D 019860 001 NDA LOPERAMIDE HYDROCHLORIDE TABLET;ORAL 2MG Yes Yes 1989/11/22 1989/11/22 J AND J CONSUMER INC Over-the-counter
IMODIUM MULTI-SYMPTOM RELIEF 020606 001 NDA LOPERAMIDE HYDROCHLORIDE; SIMETHICONE TABLET, CHEWABLE;ORAL 2MG;125MG Yes No 1997/06/26 1996/06/26 J AND J CONSUMER INC Discontinued
IMODIUM A-D EZ CHEWS 020448 001 NDA LOPERAMIDE HYDROCHLORIDE TABLET, CHEWABLE;ORAL 2MG Yes No 1997/07/24 1997/07/24 J AND J CONSUMER INC Discontinued
IMODIUM MULTI-SYMPTOM RELIEF 021140 001 NDA LOPERAMIDE HYDROCHLORIDE; SIMETHICONE TABLET;ORAL 2MG;125MG Yes Yes 2000/11/30 2000/11/30 J AND J CONSUMER INC Over-the-counter
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