药品注册申请号:017923
申请类型:NDA (新药申请)
申请人:NOVARTIS
申请人全名:NOVARTIS PHARMACEUTICALS CORP
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 MELLARIL-S THIORIDAZINE SUSPENSION;ORAL EQ 25MG HYDROCHLORIDE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** No No None 1978/10/18 Approved Prior to Jan 1, 1982 Discontinued
002 MELLARIL-S THIORIDAZINE SUSPENSION;ORAL EQ 100MG HYDROCHLORIDE/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** No No None Approved Prior to Jan 1, 1982 Discontinued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
2007/12/07 SUPPL-47(补充) Approval Labeling STANDARD
2007/12/07 SUPPL-46(补充) Approval Labeling STANDARD
2007/12/07 SUPPL-45(补充) Approval Labeling STANDARD
2007/12/07 SUPPL-42(补充) Approval Labeling STANDARD
2007/12/07 SUPPL-41(补充) Approval Labeling STANDARD
2007/12/07 SUPPL-40(补充) Approval Labeling
2007/12/07 SUPPL-39(补充) Approval Labeling
2007/12/07 SUPPL-38(补充) Approval Labeling
2007/12/07 SUPPL-37(补充) Approval Labeling
2007/12/07 SUPPL-36(补充) Approval Labeling
2007/12/07 SUPPL-34(补充) Approval Labeling
2007/12/07 SUPPL-33(补充) Approval Labeling
2007/12/07 SUPPL-24(补充) Approval Labeling
2007/12/07 SUPPL-21(补充) Approval Labeling
2007/12/07 SUPPL-20(补充) Approval Labeling
2007/12/07 SUPPL-19(补充) Approval Labeling
2007/12/07 SUPPL-18(补充) Approval Labeling
2007/12/07 SUPPL-17(补充) Approval Labeling
2007/12/07 SUPPL-13(补充) Approval Labeling
2007/12/07 SUPPL-1(补充) Approval Labeling
2001/03/15 SUPPL-49(补充) Approval Labeling STANDARD
2000/06/19 SUPPL-48(补充) Approval Labeling STANDARD
1989/05/02 SUPPL-35(补充) Approval Manufacturing (CMC) STANDARD
1988/11/15 SUPPL-23(补充) Approval Manufacturing (CMC) STANDARD
1987/08/20 SUPPL-32(补充) Approval Manufacturing (CMC) STANDARD
1987/05/26 SUPPL-31(补充) Approval Manufacturing (CMC) STANDARD
1987/04/23 SUPPL-29(补充) Approval Manufacturing (CMC) STANDARD
1987/03/13 SUPPL-28(补充) Approval Manufacturing (CMC) STANDARD
1986/11/10 SUPPL-25(补充) Approval Manufacturing (CMC) STANDARD
1986/10/06 SUPPL-27(补充) Approval Labeling
1986/10/06 SUPPL-26(补充) Approval Labeling
1986/06/10 SUPPL-22(补充) Approval Manufacturing (CMC) STANDARD
1982/09/20 SUPPL-16(补充) Approval Manufacturing (CMC) STANDARD
1982/09/13 SUPPL-15(补充) Approval Manufacturing (CMC) STANDARD
1982/04/30 SUPPL-14(补充) Approval Manufacturing (CMC) STANDARD
1981/03/18 SUPPL-11(补充) Approval Manufacturing (CMC) STANDARD
1981/01/13 SUPPL-12(补充) Approval Manufacturing (CMC) STANDARD
1981/01/09 SUPPL-10(补充) Approval Manufacturing (CMC) STANDARD
1980/04/15 SUPPL-7(补充) Approval Manufacturing (CMC) STANDARD
1980/04/15 SUPPL-2(补充) Approval Manufacturing (CMC) STANDARD
1980/04/10 SUPPL-8(补充) Approval Manufacturing (CMC) STANDARD
1979/10/15 SUPPL-6(补充) Approval REMS STANDARD
1979/10/15 SUPPL-5(补充) Approval Manufacturing (CMC) STANDARD
1979/09/11 SUPPL-3(补充) Approval Manufacturing (CMC) STANDARD
1979/06/14 SUPPL-4(补充) Approval Manufacturing (CMC) STANDARD
1978/10/18 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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