Label: TOLTRAZURIL powder

  • NDC Code(s): 58597-8559-8, 58597-8559-9
  • Packager: AMERICAN PHARMACEUTICAL INGREDIENTS LLC
  • Category: BULK INGREDIENT
  • DEA Schedule: None
  • Marketing Status: Bulk Ingredient For Animal Drug Compounding

Drug Label Information

Updated May 2, 2014

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

View All Sections
  • PRINCIPAL DISPLAY PANEL

    image description

  • INGREDIENTS AND APPEARANCE
    TOLTRAZURIL 
    toltrazuril powder
    Product Information
    Product TypeBULK INGREDIENTItem Code (Source)NDC:58597-8559
    Route of AdministrationNOT APPLICABLE
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Toltrazuril (UNII: QVZ3IAR3JS) (Toltrazuril - UNII:QVZ3IAR3JS) Toltrazuril1 g  in 1 g
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:58597-8559-81000 g in 1 BOTTLE
    2NDC:58597-8559-95000 g in 1 BOTTLE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    bulk ingredient for animal drug compounding05/02/2014
    Labeler - AMERICAN PHARMACEUTICAL INGREDIENTS LLC (078793641)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

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