Label: BUDESONIDE powder

  • NDC Code(s): 73377-005-01, 73377-005-02, 73377-005-03, 73377-005-05
  • Packager: AX Pharmaceutical Corp
  • Category: BULK INGREDIENT - ANIMAL DRUG

Drug Label Information

Updated February 5, 2024

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

  • Budesonide

    image descriptionimage descriptionimage descriptionimage description

  • INGREDIENTS AND APPEARANCE
    BUDESONIDE 
    budesonide powder
    Product Information
    Product TypeItem Code (Source)NDC:73377-005
    Route of AdministrationNOT APPLICABLE
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BUDESONIDE (UNII: Q3OKS62Q6X) (BUDESONIDE - UNII:Q3OKS62Q6X) BUDESONIDE1 g  in 1 g
    Product Characteristics
    ColorwhiteScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73377-005-01500 g in 1 JAR
    2NDC:73377-005-02100 g in 1 JAR
    3NDC:73377-005-0325 g in 1 JAR
    4NDC:73377-005-0514.1 g in 1 PACKAGE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    bulk ingredient for animal drug compounding01/23/2020
    Labeler - AX Pharmaceutical Corp (204011316)
    Establishment
    NameAddressID/FEIBusiness Operations
    AX Pharmaceutical Corp204011316repack, relabel