Label: BENAZEPRIL HYDROCHLORIDE powder

  • NDC Code(s): 73377-060-01, 73377-060-02, 73377-060-03, 73377-060-04, view more
    73377-060-05
  • Packager: AX Pharmaceutical Corp
  • Category: BULK INGREDIENT - ANIMAL DRUG
  • DEA Schedule: None
  • Marketing Status: bulk ingredient

Drug Label Information

Updated January 22, 2025

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  • Benazepril Hydrochloride

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  • INGREDIENTS AND APPEARANCE
    BENAZEPRIL HYDROCHLORIDE 
    benazepril hydrochloride powder
    Product Information
    Product TypeItem Code (Source)NDC:73377-060
    Route of AdministrationNOT APPLICABLE
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENAZEPRIL HYDROCHLORIDE (UNII: N1SN99T69T) (BENAZEPRIL HYDROCHLORIDE - UNII:N1SN99T69T) BENAZEPRIL HYDROCHLORIDE1 g  in 1 g
    Product Characteristics
    ColorwhiteScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73377-060-01500 g in 1 JAR
    2NDC:73377-060-02100 g in 1 JAR
    3NDC:73377-060-031000 g in 1 JAR
    4NDC:73377-060-0450 g in 1 JAR
    5NDC:73377-060-0592 g in 1 JAR
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    bulk ingredient07/09/2020
    Labeler - AX Pharmaceutical Corp (204011316)
    Establishment
    NameAddressID/FEIBusiness Operations
    AX Pharmaceutical Corp204011316repack, relabel