药品注册申请号:017862
申请类型:NDA (新药申请)
申请人:HIKMA
申请人全名:HIKMA PHARMACEUTICALS USA INC
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 REGLAN METOCLOPRAMIDE HYDROCHLORIDE INJECTABLE;INJECTION EQ 5MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** Yes No None 1979/02/07 Approved Prior to Jan 1, 1982 Discontinued
004 REGLAN METOCLOPRAMIDE HYDROCHLORIDE INJECTABLE;INJECTION EQ 10MG BASE/ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** No No None 1987/05/28 Discontinued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
2010/11/18 SUPPL-63(补充) Approval Labeling UNKNOWN
2009/06/30 SUPPL-61(补充) Approval Labeling 901 REQUIRED
2004/04/19 SUPPL-51(补充) Approval Labeling STANDARD
2004/04/19 SUPPL-50(补充) Approval Labeling STANDARD
2001/11/07 SUPPL-48(补充) Approval Labeling STANDARD
2001/01/29 SUPPL-47(补充) Approval Manufacturing (CMC) PRIORITY
2001/01/22 SUPPL-46(补充) Approval Manufacturing (CMC) PRIORITY
2001/01/22 SUPPL-45(补充) Approval Manufacturing (CMC) PRIORITY
2000/06/01 SUPPL-40(补充) Approval Labeling STANDARD
1999/08/27 SUPPL-43(补充) Approval Manufacturing (CMC) PRIORITY
1999/03/09 SUPPL-42(补充) Approval Labeling STANDARD
1998/01/30 SUPPL-41(补充) Approval Manufacturing (CMC) PRIORITY
1996/06/24 SUPPL-39(补充) Approval Labeling STANDARD
1994/05/31 SUPPL-38(补充) Approval Labeling STANDARD
1992/08/31 SUPPL-35(补充) Approval Manufacturing (CMC) PRIORITY
1990/02/16 SUPPL-37(补充) Approval Manufacturing (CMC) PRIORITY
1989/02/22 SUPPL-36(补充) Approval Labeling
1988/09/12 SUPPL-33(补充) Approval Manufacturing (CMC) PRIORITY
1987/09/15 SUPPL-32(补充) Approval Labeling
1987/05/28 SUPPL-29(补充) Approval Manufacturing (CMC) PRIORITY
1987/05/28 SUPPL-21(补充) Approval Efficacy
1987/04/17 SUPPL-31(补充) Approval Manufacturing (CMC) PRIORITY
1986/10/23 SUPPL-30(补充) Approval Labeling
1985/11/20 SUPPL-26(补充) Approval Manufacturing (CMC) PRIORITY
1985/10/21 SUPPL-25(补充) Approval Labeling
1985/08/20 SUPPL-24(补充) Approval Labeling
1985/03/12 SUPPL-22(补充) Approval Labeling
1984/08/03 SUPPL-18(补充) Approval Manufacturing (CMC) PRIORITY
1983/07/05 SUPPL-20(补充) Approval Efficacy
1983/06/14 SUPPL-19(补充) Approval Manufacturing (CMC) PRIORITY
1983/04/13 SUPPL-17(补充) Approval Labeling
1983/01/04 SUPPL-16(补充) Approval Manufacturing (CMC) PRIORITY
1982/11/12 SUPPL-15(补充) Approval Labeling
1982/11/02 SUPPL-14(补充) Approval Manufacturing (CMC) PRIORITY
1982/09/08 SUPPL-13(补充) Approval Labeling
1982/06/28 SUPPL-6(补充) Approval Efficacy
1982/06/23 SUPPL-12(补充) Approval Manufacturing (CMC) PRIORITY
1982/05/27 SUPPL-10(补充) Approval Manufacturing (CMC) PRIORITY
1982/02/19 SUPPL-9(补充) Approval Efficacy
1981/12/09 SUPPL-8(补充) Approval Manufacturing (CMC) PRIORITY
1981/10/08 SUPPL-7(补充) Approval Manufacturing (CMC) PRIORITY
1981/01/22 SUPPL-3(补充) Approval Efficacy
1980/01/25 SUPPL-5(补充) Approval Manufacturing (CMC) PRIORITY
1979/12/28 SUPPL-4(补充) Approval Labeling
1979/10/16 SUPPL-2(补充) Approval Manufacturing (CMC) PRIORITY
1979/10/01 SUPPL-1(补充) Approval Labeling
1979/02/07 ORIG-1(原始申请) Approval Type 1 - New Molecular Entity PRIORITY
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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