美国FDA药品数据库(U.S. FDA Drugs Database)
检索条件:" 药品名称=NORINYL"
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
NORINYL 1+50 21-DAY 013625 002 NDA MESTRANOL; NORETHINDRONE TABLET;ORAL-21 0.05MG;1MG No No 1964/03/05 Approved Prior to Jan 1, 1982 ACTAVIS LABS UT INC Discontinued
NORINYL 013625 004 NDA MESTRANOL; NORETHINDRONE TABLET;ORAL-20 0.1MG;2MG No No 1964/03/05 Approved Prior to Jan 1, 1982 ACTAVIS LABS UT INC Discontinued
NORINYL 1+50 28-DAY 016659 001 NDA MESTRANOL; NORETHINDRONE TABLET;ORAL-28 0.05MG;1MG Yes No 1967/11/17 Approved Prior to Jan 1, 1982 ACTAVIS LABS UT INC Discontinued
NORINYL 1+80 21-DAY 016724 001 NDA MESTRANOL; NORETHINDRONE TABLET;ORAL-21 0.08MG;1MG No No 1968/11/06 Approved Prior to Jan 1, 1982 GD SEARLE LLC Discontinued
NORINYL 1+80 28-DAY 016725 001 NDA MESTRANOL; NORETHINDRONE TABLET;ORAL-28 0.08MG;1MG No No 1968/11/08 Approved Prior to Jan 1, 1982 GD SEARLE LLC Discontinued
NORINYL 1+35 21-DAY 017565 001 NDA ETHINYL ESTRADIOL; NORETHINDRONE TABLET;ORAL-21 0.035MG;1MG No No 1974/12/27 Approved Prior to Jan 1, 1982 ALLERGAN Discontinued
NORINYL 1+35 28-DAY 017565 002 NDA ETHINYL ESTRADIOL; NORETHINDRONE TABLET;ORAL-28 0.035MG;1MG No No 1974/12/27 Approved Prior to Jan 1, 1982 ALLERGAN Discontinued
TRI-NORINYL 21-DAY 018977 001 NDA ETHINYL ESTRADIOL; NORETHINDRONE TABLET;ORAL-21 0.035MG,0.035MG,0.035MG;0.5MG,1MG,0.5MG No No 1984/04/11 1984/04/13 DR REDDYS LABS SA Discontinued
TRI-NORINYL 28-DAY 018977 002 NDA ETHINYL ESTRADIOL; NORETHINDRONE TABLET;ORAL-28 0.035MG,0.035MG,0.035MG;0.5MG,1MG,0.5MG Yes Yes 1984/04/11 1984/04/13 DR REDDYS LABS SA Prescription
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