药品注册申请号:018439
申请类型:NDA (新药申请)
申请人:WATSON LABS
申请人全名:WATSON 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
002 MVC PLUS ASCORBIC ACID; BIOTIN; CYANOCOBALAMIN; DEXPANTHENOL; ERGOCALCIFEROL; FOLIC ACID; NIACINAMIDE; PYRIDOXINE HYDROCHLORIDE; RIBOFLAVIN 5'-PHOSPHATE SODIUM; THIAMINE HYDROCHLORIDE; VITAMIN A; VITAMIN E INJECTABLE;INJECTION 10MG/ML;0.006MG/ML;0.5MCG/ML;1.5MG/ML;20 IU/ML;0.04MG/ML;4MG/ML;0.4MG/ML;0.36MG/ML;0.3MG/ML;330 UNITS/ML;1 IU/ML No No None 1982/07/13 1985/08/08 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
1999/02/10 SUPPL-20(补充) Approval Manufacturing (CMC) STANDARD
1998/07/16 SUPPL-19(补充) Approval Manufacturing (CMC) STANDARD
1998/02/26 SUPPL-18(补充) Approval Manufacturing (CMC) STANDARD
1997/09/26 SUPPL-17(补充) Approval Manufacturing (CMC) STANDARD
1996/12/24 SUPPL-15(补充) Approval Manufacturing (CMC) STANDARD
1996/12/10 SUPPL-16(补充) Approval Manufacturing (CMC) STANDARD
1996/02/27 SUPPL-14(补充) Approval Labeling STANDARD
1994/10/14 SUPPL-13(补充) Approval Manufacturing (CMC) STANDARD
1993/11/01 SUPPL-12(补充) Approval Manufacturing (CMC) STANDARD
1989/12/05 SUPPL-10(补充) Approval Manufacturing (CMC) STANDARD
1986/08/29 SUPPL-8(补充) Approval Manufacturing (CMC) STANDARD
1985/05/14 SUPPL-2(补充) Approval Manufacturing (CMC) STANDARD
1983/01/17 SUPPL-1(补充) Approval Manufacturing (CMC) STANDARD
1982/07/13 ORIG-1(原始申请) Approval Type 5 - New Formulation or New Manufacturer 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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药品NDC数据与药品包装、标签说明书
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