美国FDA药品数据库（U.S. FDA Drugs Database）
检索条件:" 药品名称=DARVON"
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
DARVON 010997 001 NDA PROPOXYPHENE HYDROCHLORIDE CAPSULE;ORAL 32MG No No 1957/08/16 Approved Prior to Jan 1, 1982 XANODYNE PHARM Discontinued
DARVON 010997 003 NDA PROPOXYPHENE HYDROCHLORIDE CAPSULE;ORAL 65MG No No 1957/08/16 Approved Prior to Jan 1, 1982 XANODYNE PHARM Discontinued
DARVON W/ ASA 010996 005 NDA ASPIRIN; PROPOXYPHENE HYDROCHLORIDE CAPSULE;ORAL 325MG;65MG No No 1957/11/12 Approved Prior to Jan 1, 1982 XANODYNE PHARM Discontinued
DARVON COMPOUND 010996 006 NDA ASPIRIN; CAFFEINE; PROPOXYPHENE HYDROCHLORIDE CAPSULE;ORAL 389MG;32.4MG;32MG No No 1957/11/12 1983/03/08 XANODYNE PHARM Discontinued
DARVON COMPOUND-65 010996 007 NDA ASPIRIN; CAFFEINE; PROPOXYPHENE HYDROCHLORIDE CAPSULE;ORAL 389MG;32.4MG;65MG No No 1957/11/12 1983/03/08 XANODYNE PHARM Discontinued
DARVON-N W/ ASA 016829 001 NDA ASPIRIN; PROPOXYPHENE NAPSYLATE CAPSULE;ORAL 325MG;100MG No No 1971/09/09 Approved Prior to Jan 1, 1982 AAIPHARMA LLC Discontinued
DARVON-N 016861 001 NDA PROPOXYPHENE NAPSYLATE SUSPENSION;ORAL 50MG/5ML No No 1971/09/09 Approved Prior to Jan 1, 1982 AAIPHARMA LLC Discontinued
DARVON-N 016862 002 NDA PROPOXYPHENE NAPSYLATE TABLET;ORAL 100MG No No 1971/09/09 Approved Prior to Jan 1, 1982 XANODYNE PHARM Discontinued
DARVON-N W/ ASA 016863 001 NDA ASPIRIN; PROPOXYPHENE NAPSYLATE TABLET;ORAL 325MG;100MG No No 1971/09/09 Approved Prior to Jan 1, 1982 AAIPHARMA LLC Discontinued
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