美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=ACETAMINOPHEN"
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
PROPOXYPHENE NAPSYLATE AND ACETAMINOPHEN 070398 001 ANDA ACETAMINOPHEN; PROPOXYPHENE NAPSYLATE TABLET;ORAL 325MG;50MG No No -- 1986/12/18 WATSON LABS Discontinued
PROPOXYPHENE NAPSYLATE AND ACETAMINOPHEN 070399 001 ANDA ACETAMINOPHEN; PROPOXYPHENE NAPSYLATE TABLET;ORAL 650MG;100MG No No -- 1986/12/18 WATSON LABS Discontinued
PROPOXYPHENE NAPSYLATE AND ACETAMINOPHEN 070732 001 ANDA ACETAMINOPHEN; PROPOXYPHENE NAPSYLATE TABLET;ORAL 650MG;100MG No No -- 1986/01/03 TEVA Discontinued
PROPOXYPHENE NAPSYLATE AND ACETAMINOPHEN 072106 001 ANDA ACETAMINOPHEN; PROPOXYPHENE NAPSYLATE TABLET;ORAL 650MG;100MG No No -- 1988/05/13 HALSEY Discontinued
ACETAMINOPHEN 073106 001 ANDA ACETAMINOPHEN SUPPOSITORY;RECTAL 120MG No No -- 1995/02/27 ABLE Discontinued
ACETAMINOPHEN 073107 001 ANDA ACETAMINOPHEN SUPPOSITORY;RECTAL 325MG No No -- 1995/02/27 ABLE Discontinued
ACETAMINOPHEN 073108 001 ANDA ACETAMINOPHEN SUPPOSITORY;RECTAL 650MG No No -- 1995/02/27 ABLE Discontinued
ACETAMINOPHEN AND CODEINE PHOSPHATE 083871 001 ANDA ACETAMINOPHEN; CODEINE PHOSPHATE TABLET;ORAL 300MG;15MG No No -- Approved Prior to Jan 1, 1982 HALSEY Discontinued
ACETAMINOPHEN AND CODEINE PHOSPHATE 083872 001 ANDA ACETAMINOPHEN; CODEINE PHOSPHATE TABLET;ORAL 300MG;30MG No No -- Approved Prior to Jan 1, 1982 HALSEY Discontinued
ACETAMINOPHEN AND CODEINE PHOSPHATE 085676 001 ANDA ACETAMINOPHEN; CODEINE PHOSPHATE TABLET;ORAL 300MG;30MG No No -- Approved Prior to Jan 1, 1982 VITARINE Discontinued
ACETAMINOPHEN AND CODEINE PHOSPHATE 086549 001 ANDA ACETAMINOPHEN; CODEINE PHOSPHATE TABLET;ORAL 300MG;60MG No No -- Approved Prior to Jan 1, 1982 HALSEY Discontinued
ACETAMINOPHEN AND CODEINE PHOSPHATE 087141 001 ANDA ACETAMINOPHEN; CODEINE PHOSPHATE TABLET;ORAL 300MG;30MG No No -- Approved Prior to Jan 1, 1982 LEDERLE Discontinued
BUTALBITAL, ACETAMINOPHEN AND CAFFEINE 087629 001 ANDA ACETAMINOPHEN; BUTALBITAL; CAFFEINE TABLET;ORAL 325MG;50MG;40MG No No -- 1984/11/13 GILBERT LABS Discontinued
BUTALBITAL, ACETAMINOPHEN AND CAFFEINE 088825 001 ANDA ACETAMINOPHEN; BUTALBITAL; CAFFEINE CAPSULE;ORAL 325MG;50MG;40MG **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons** No No -- 1984/12/05 GILBERT LABS Discontinued
HYDROCODONE BITARTRATE AND ACETAMINOPHEN 089290 001 ANDA ACETAMINOPHEN; HYDROCODONE BITARTRATE TABLET;ORAL 500MG;5MG No No -- 1987/05/29 USL PHARMA Discontinued
HYDROCODONE BITARTRATE AND ACETAMINOPHEN 089291 001 ANDA ACETAMINOPHEN; HYDROCODONE BITARTRATE TABLET;ORAL 500MG;5MG No No -- 1987/05/29 USL PHARMA Discontinued
HYDROCODONE BITARTRATE AND ACETAMINOPHEN 089554 001 ANDA ACETAMINOPHEN; HYDROCODONE BITARTRATE TABLET;ORAL 500MG;5MG No No -- 1987/06/12 HALSEY Discontinued
BUTALBITAL AND ACETAMINOPHEN 089568 001 ANDA ACETAMINOPHEN; BUTALBITAL TABLET;ORAL 325MG;50MG No No -- 1988/10/05 HALSEY Discontinued
PROPOXYPHENE HYDROCHLORIDE AND ACETAMINOPHEN 083689 001 ANDA ACETAMINOPHEN; PROPOXYPHENE HYDROCHLORIDE TABLET;ORAL 325MG;32MG No No 1974/10/25 Approved Prior to Jan 1, 1982 MYLAN Discontinued
PROPOXYPHENE HYDROCHLORIDE AND ACETAMINOPHEN 083978 001 ANDA ACETAMINOPHEN; PROPOXYPHENE HYDROCHLORIDE TABLET;ORAL 650MG;65MG No No 1974/10/25 Approved Prior to Jan 1, 1982 MYLAN Discontinued
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