药品注册申请号:017802
申请类型:NDA (新药申请)
申请人:WYETH PHARMS
申请人全名:WYETH PHARMACEUTICALS LLC
产品信息
产品号商品名活性成分剂型/给药途径规格/剂量参比药物(RLD)生物等效参考标准(RS)治疗等效代码该申请号批准日期该产品号批准日期市场状态
001 LO/OVRAL-28 ETHINYL ESTRADIOL; NORGESTREL TABLET;ORAL-28 0.03MG;0.3MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No None 1976/03/16 Approved Prior to Jan 1, 1982 Discontinued
批准日期,申请提交历史,通知信,药品说明书,审评文件等信息
提交状态日期提交号审批结论申请内容分类审评优先级;罕用药状态通知信、审评文件、说明书、包装标签备注
2022/04/29 SUPPL-35(补充) Approval Labeling STANDARD
2019/05/08 SUPPL-34(补充) Approval Labeling STANDARD
2018/03/20 SUPPL-33(补充) Approval Labeling STANDARD
2017/08/09 SUPPL-32(补充) Approval Labeling STANDARD
2017/06/08 SUPPL-29(补充) Approval Labeling STANDARD
2002/03/06 SUPPL-22(补充) Approval Manufacturing (CMC) STANDARD
2000/04/03 SUPPL-18(补充) Approval Labeling STANDARD
1998/07/08 SUPPL-20(补充) Approval Manufacturing (CMC) STANDARD
1994/11/29 SUPPL-16(补充) Approval Labeling STANDARD
1994/01/28 SUPPL-17(补充) Approval Labeling STANDARD
1993/12/23 SUPPL-15(补充) Approval Manufacturing (CMC) STANDARD
1990/08/08 SUPPL-13(补充) Approval Labeling
1988/04/27 SUPPL-14(补充) Approval Manufacturing (CMC) STANDARD
1986/07/15 SUPPL-11(补充) Approval Labeling
1986/02/19 SUPPL-10(补充) Approval Manufacturing (CMC) STANDARD
1985/10/16 SUPPL-9(补充) Approval Labeling
1985/04/05 SUPPL-6(补充) Approval Manufacturing (CMC) STANDARD
1984/09/04 SUPPL-8(补充) Approval Manufacturing (CMC) STANDARD
1984/07/26 SUPPL-7(补充) Approval Labeling
1979/01/08 SUPPL-2(补充) Approval Labeling
1977/12/08 SUPPL-3(补充) Approval Labeling
1976/03/16 ORIG-1(原始申请) Approval Type 3 - New Dosage Form STANDARD
与本品相关的专利信息(来自FDA橙皮书Orange Book)
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与本品相关的市场独占权保护信息
关联产品号独占权代码失效日期备注
与本品治疗等效的药品
本品无治疗等效药品
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