Label: CETIRIZINE DIHYDROCHLORIDE powder

  • NDC Code(s): 73377-046-01, 73377-046-02, 73377-046-03
  • Packager: AX Pharmaceutical Corp
  • Category: BULK INGREDIENT - ANIMAL DRUG
  • DEA Schedule: None
  • Marketing Status: Bulk Ingredient For Animal Drug Compounding

Drug Label Information

Updated November 10, 2023

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  • Cetirizine Dihydrochloride

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  • INGREDIENTS AND APPEARANCE
    CETIRIZINE DIHYDROCHLORIDE 
    cetirizine dihydrochloride powder
    Product Information
    Product TypeItem Code (Source)NDC:73377-046
    Route of AdministrationNOT APPLICABLE
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    CETIRIZINE HYDROCHLORIDE (UNII: 64O047KTOA) (CETIRIZINE HYDROCHLORIDE - UNII:64O047KTOA) CETIRIZINE HYDROCHLORIDE1 g  in 1 g
    Product Characteristics
    ColorwhiteScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73377-046-01500 g in 1 JAR
    2NDC:73377-046-02100 g in 1 JAR
    3NDC:73377-046-035000 g in 1 JAR
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    bulk ingredient for animal drug compounding04/17/2020
    Labeler - AX Pharmaceutical Corp (204011316)
    Establishment
    NameAddressID/FEIBusiness Operations
    AX Pharmaceutical Corp204011316repack, relabel
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Safety

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Clinical Trials, PubMed, Biochemical Data Summary

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