美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=HYDROCORTISONE"
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
HYDROCORTISONE AND ACETIC ACID 040097 001 ANDA ACETIC ACID, GLACIAL; HYDROCORTISONE SOLUTION/DROPS;OTIC 2%;1% No No -- 1994/10/31 BAUSCH AND LOMB Discontinued
BACITRACIN-NEOMYCIN-POLYMYXIN W/ HYDROCORTISONE ACETATE 060731 002 ANDA BACITRACIN; HYDROCORTISONE ACETATE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE OINTMENT;OPHTHALMIC 400 UNITS/GM;1%;EQ 3.5MG BASE/GM;10,000 UNITS/GM No No -- Approved Prior to Jan 1, 1982 ALTANA Discontinued
NEOMYCIN & POLYMYXIN B SULFATES & BACITRACIN ZINC & HYDROCORTISONE 062381 001 ANDA BACITRACIN ZINC; HYDROCORTISONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE OINTMENT;TOPICAL 400 UNITS/GM;1%;EQ 3.5MG BASE/GM;5,000 UNITS/GM No No -- 1985/09/06 PHARMAFAIR Discontinued
ZINC BACITRACIN,NEOMYCIN SULFATE,POLYMYXIN B SULFATE & HYDROCORTISONE 062389 001 ANDA BACITRACIN ZINC; HYDROCORTISONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE OINTMENT;OPHTHALMIC 400 UNITS/GM;1%;EQ 3.5MG BASE/GM;10,000 UNITS/GM No No -- 1982/07/02 PHARMAFAIR Discontinued
NEOMYCIN SULFATE-POLYMYXIN B SULFATE-HYDROCORTISONE 062394 001 ANDA HYDROCORTISONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE SOLUTION/DROPS;OTIC 1%;EQ 3.5MG BASE/ML;10,000 UNITS/ML No No -- 1982/09/29 PHARMAFAIR Discontinued
NEOMYCIN SULFATE, POLYMYXIN B SULFATE & HYDROCORTISONE 062617 001 ANDA HYDROCORTISONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE SUSPENSION/DROPS;OTIC 1%;EQ 3.5MG BASE/ML;10,000 UNITS/ML No No -- 1985/09/18 PHARMAFAIR Discontinued
NEOMYCIN SULFATE-POLYMYXIN B SULFATE-HYDROCORTISONE 062623 001 ANDA HYDROCORTISONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE SUSPENSION/DROPS;OPHTHALMIC 1%;EQ 3.5MG BASE/ML;10,000 UNITS/ML No No -- 1985/09/24 PHARMAFAIR Discontinued
HYDROCORTISONE 080395 001 ANDA HYDROCORTISONE TABLET;ORAL 20MG No No -- Approved Prior to Jan 1, 1982 PUREPAC PHARM Discontinued
HYDROCORTISONE ACETATE 080419 001 ANDA HYDROCORTISONE ACETATE CREAM;TOPICAL 1% No No -- 1982/01/25 CENCI Discontinued
HYDROCORTISONE 080452 001 ANDA HYDROCORTISONE CREAM;TOPICAL 0.5% No No -- Approved Prior to Jan 1, 1982 EVERYLIFE Discontinued
HYDROCORTISONE 080452 002 ANDA HYDROCORTISONE CREAM;TOPICAL 1% No No -- Approved Prior to Jan 1, 1982 EVERYLIFE Discontinued
HYDROCORTISONE 080456 002 ANDA HYDROCORTISONE CREAM;TOPICAL 0.5% No No -- Approved Prior to Jan 1, 1982 INGRAM PHARM Discontinued
HYDROCORTISONE 080456 003 ANDA HYDROCORTISONE CREAM;TOPICAL 1% No No -- Approved Prior to Jan 1, 1982 INGRAM PHARM Discontinued
HYDROCORTISONE 080489 002 ANDA HYDROCORTISONE OINTMENT;TOPICAL 0.5% No No -- Approved Prior to Jan 1, 1982 ALTANA Discontinued
HYDROCORTISONE 080489 003 ANDA HYDROCORTISONE OINTMENT;TOPICAL 1% No No -- Approved Prior to Jan 1, 1982 ALTANA Discontinued
HYDROCORTISONE 080624 001 ANDA HYDROCORTISONE TABLET;ORAL 20MG No No -- Approved Prior to Jan 1, 1982 ELKINS SINN Discontinued
HYDROCORTISONE 080732 001 ANDA HYDROCORTISONE TABLET;ORAL 20MG No No -- Approved Prior to Jan 1, 1982 INWOOD LABS Discontinued
HYDROCORTISONE 080781 001 ANDA HYDROCORTISONE TABLET;ORAL 20MG No No -- Approved Prior to Jan 1, 1982 IMPAX LABS Discontinued
HYDROCORTISONE 080848 002 ANDA HYDROCORTISONE CREAM;TOPICAL 0.5% No No -- Approved Prior to Jan 1, 1982 ALTANA Discontinued
HYDROCORTISONE 080848 003 ANDA HYDROCORTISONE CREAM;TOPICAL 1% No No -- Approved Prior to Jan 1, 1982 ALTANA Discontinued
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