Label: TRILOSTANE powder

  • NDC Code(s): 73377-027-01, 73377-027-02, 73377-027-03
  • Packager: AX Pharmaceutical Corp
  • Category: BULK INGREDIENT - ANIMAL DRUG
  • DEA Schedule: None
  • Marketing Status: Bulk Ingredient For Animal Drug Compounding

Drug Label Information

Updated September 23, 2022

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  • Trilostane

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  • INGREDIENTS AND APPEARANCE
    TRILOSTANE 
    trilostane powder
    Product Information
    Product TypeItem Code (Source)NDC:73377-027
    Route of AdministrationNOT APPLICABLE
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TRILOSTANE (UNII: L0FPV48Q5R) (TRILOSTANE - UNII:L0FPV48Q5R) TRILOSTANE1 kg  in 1 kg
    Product Characteristics
    ColorwhiteScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73377-027-011 kg in 1 JAR
    2NDC:73377-027-020.5 kg in 1 JAR
    3NDC:73377-027-030.1 kg in 1 JAR
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    bulk ingredient for animal drug compounding09/23/2022
    Labeler - AX Pharmaceutical Corp (204011316)
    Establishment
    NameAddressID/FEIBusiness Operations
    AX Pharmaceutical Corp204011316repack, relabel
    Establishment
    NameAddressID/FEIBusiness Operations
    Zhejiang Xianju Junye Pharmaceutical Co., Ltd.(Yangfu site)421340422api manufacture
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Safety

Report Adverse Events (Animal Drug), FDA Safety Recalls (Animal Drug)

Related Resources

Clinical Trials, PubMed, Biochemical Data Summary

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