Label: IDOXURIDINE powder

  • NDC Code(s): 71052-140-01, 71052-140-02, 71052-140-10, 71052-140-25
  • Packager: DARMERICA, LLC
  • Category: BULK INGREDIENT - ANIMAL DRUG
  • DEA Schedule: None
  • Marketing Status: Bulk Ingredient For Animal Drug Compounding

Drug Label Information

Updated March 18, 2024

If you are a consumer or patient please visit this version.

View All Sections
  • Idoxuridine

    Idoxuridine

  • INGREDIENTS AND APPEARANCE
    IDOXURIDINE 
    idoxuridine powder
    Product Information
    Product TypeItem Code (Source)NDC:71052-140
    Route of AdministrationNOT APPLICABLE
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Idoxuridine (UNII: LGP81V5245) (IDOXURIDINE - UNII:LGP81V5245) Idoxuridine1 kg  in 1 kg
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71052-140-100.1 kg in 1 PACKAGE
    2NDC:71052-140-250.025 kg in 1 PACKAGE
    3NDC:71052-140-020.005 kg in 1 PACKAGE
    4NDC:71052-140-010.001 kg in 1 PACKAGE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    bulk ingredient for animal drug compounding01/25/2023
    Labeler - DARMERICA, LLC (080233052)
View All Sections

Find additional resources

(also available in the left menu)

Safety

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

Related Resources

Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!