药品注册申请号:088764
申请类型:ANDA (仿制药申请)
申请人:NOSTRUM LABS INC
申请人全名:NOSTRUM LABORATORIES 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 PROMETH VC W/ CODEINE CODEINE PHOSPHATE; PHENYLEPHRINE HYDROCHLORIDE; PROMETHAZINE HYDROCHLORIDE SYRUP;ORAL 10MG/5ML;5MG/5ML;6.25MG/5ML No No None 1984/10/31 1984/10/31 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
2023/12/15 SUPPL-89(补充) Approval Labeling STANDARD
2018/06/28 SUPPL-88(补充) Approval Labeling STANDARD
2018/06/08 SUPPL-87(补充) Approval Labeling STANDARD
2017/08/29 SUPPL-86(补充) Approval Labeling STANDARD
2017/01/13 SUPPL-85(补充) Approval Labeling STANDARD
2013/05/10 SUPPL-84(补充) Approval Labeling STANDARD
2013/05/03 SUPPL-81(补充) Approval Labeling
2011/08/01 SUPPL-75(补充) Approval Labeling
2009/03/20 SUPPL-77(补充) Approval Labeling
2005/10/06 SUPPL-63(补充) Approval Labeling
2005/05/02 SUPPL-53(补充) Approval Labeling
2003/06/06 SUPPL-49(补充) Approval Labeling
2002/07/15 SUPPL-48(补充) Approval Manufacturing (CMC)
2001/10/03 SUPPL-47(补充) Approval Manufacturing (CMC)
2001/10/03 SUPPL-46(补充) Approval Manufacturing (CMC)
2000/10/02 SUPPL-45(补充) Approval Manufacturing (CMC)
1998/12/01 SUPPL-42(补充) Approval Manufacturing (CMC)
1998/11/05 SUPPL-41(补充) Approval Manufacturing (CMC)
1998/11/05 SUPPL-40(补充) Approval Manufacturing (CMC)
1998/11/05 SUPPL-39(补充) Approval Manufacturing (CMC)
1997/09/02 SUPPL-37(补充) Approval Manufacturing (CMC)
1997/04/07 SUPPL-36(补充) Approval Manufacturing (CMC)
1996/06/18 SUPPL-35(补充) Approval Manufacturing (CMC)
1996/05/30 SUPPL-28(补充) Approval Manufacturing (CMC)
1996/05/30 SUPPL-27(补充) Approval Manufacturing (CMC)
1996/05/07 SUPPL-34(补充) Approval Labeling
1996/05/07 SUPPL-33(补充) Approval Manufacturing (CMC)
1996/05/07 SUPPL-32(补充) Approval Manufacturing (CMC)
1996/05/07 SUPPL-30(补充) Approval Manufacturing (CMC)
1996/05/07 SUPPL-29(补充) Approval Manufacturing (CMC)
1995/10/23 SUPPL-31(补充) Approval Manufacturing (CMC)
1994/02/02 SUPPL-26(补充) Approval Manufacturing (CMC)
1992/06/12 SUPPL-25(补充) Approval Labeling
1991/02/08 SUPPL-21(补充) Approval Labeling
1991/01/23 SUPPL-23(补充) Approval Manufacturing (CMC)
1990/10/03 SUPPL-17(补充) Approval Manufacturing (CMC)
1990/10/03 SUPPL-16(补充) Approval Manufacturing (CMC)
1990/10/03 SUPPL-15(补充) Approval Manufacturing (CMC)
1990/09/28 SUPPL-22(补充) Approval Manufacturing (CMC)
1990/03/29 SUPPL-20(补充) Approval Labeling
1990/02/07 SUPPL-19(补充) Approval Labeling
1989/11/06 SUPPL-18(补充) Approval Labeling
1988/12/15 SUPPL-14(补充) Approval Manufacturing (CMC)
1988/12/09 SUPPL-13(补充) Approval Manufacturing (CMC)
1987/04/28 SUPPL-5(补充) Approval Manufacturing (CMC)
1987/04/28 SUPPL-4(补充) Approval Manufacturing (CMC)
1987/03/17 SUPPL-9(补充) Approval Manufacturing (CMC)
1986/06/19 SUPPL-7(补充) Approval Manufacturing (CMC)
1986/02/18 SUPPL-3(补充) Approval Manufacturing (CMC)
1985/08/14 SUPPL-2(补充) Approval Manufacturing (CMC)
1984/10/31 ORIG-1(原始申请) Approval
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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