美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=NEO-CORTEF"
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
NEO-CORTEF 060610 001 ANDA HYDROCORTISONE ACETATE; NEOMYCIN SULFATE OINTMENT;OPHTHALMIC 0.5%;EQ 3.5MG BASE/GM No No -- Approved Prior to Jan 1, 1982 PHARMACIA AND UPJOHN Discontinued
NEO-CORTEF 060610 002 ANDA HYDROCORTISONE ACETATE; NEOMYCIN SULFATE OINTMENT;OPHTHALMIC 1.5%;EQ 3.5MG BASE/GM No No -- Approved Prior to Jan 1, 1982 PHARMACIA AND UPJOHN Discontinued
NEO-CORTEF 060612 001 ANDA HYDROCORTISONE ACETATE; NEOMYCIN SULFATE SUSPENSION/DROPS;OPHTHALMIC 1.5%;EQ 3.5MG BASE/ML No No -- Approved Prior to Jan 1, 1982 PHARMACIA AND UPJOHN Discontinued
NEO-CORTEF 060612 002 ANDA HYDROCORTISONE ACETATE; NEOMYCIN SULFATE SUSPENSION/DROPS;OPHTHALMIC 0.5%;EQ 3.5MG BASE/ML No No -- Approved Prior to Jan 1, 1982 PHARMACIA AND UPJOHN Discontinued
NEO-CORTEF 061049 001 ANDA HYDROCORTISONE ACETATE; NEOMYCIN SULFATE CREAM;TOPICAL 1%;EQ 3.5MG BASE/GM No No -- Approved Prior to Jan 1, 1982 PHARMACIA AND UPJOHN Discontinued
NEO-CORTEF 061049 002 ANDA HYDROCORTISONE ACETATE; NEOMYCIN SULFATE CREAM;TOPICAL 2.5%;EQ 3.5MG BASE/GM No No -- Approved Prior to Jan 1, 1982 PHARMACIA AND UPJOHN Discontinued
NEO-CORTEF 060751 001 ANDA HYDROCORTISONE ACETATE; NEOMYCIN SULFATE OINTMENT;TOPICAL 0.5%;EQ 3.5MG BASE/GM No No 1965/05/18 Approved Prior to Jan 1, 1982 PHARMACIA AND UPJOHN Discontinued
NEO-CORTEF 060751 002 ANDA HYDROCORTISONE ACETATE; NEOMYCIN SULFATE OINTMENT;TOPICAL 1%;EQ 3.5MG BASE/GM No No 1965/05/18 Approved Prior to Jan 1, 1982 PHARMACIA AND UPJOHN Discontinued
NEO-CORTEF 060751 003 ANDA HYDROCORTISONE ACETATE; NEOMYCIN SULFATE OINTMENT;TOPICAL 2.5%;EQ 3.5MG BASE/GM No No 1965/05/18 Approved Prior to Jan 1, 1982 PHARMACIA AND UPJOHN Discontinued
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