Label: PONAZURIL powder

  • NDC Code(s): 10695-093-50
  • Packager: Willow Birch Pharma, Inc.
  • Category: BULK INGREDIENT
  • DEA Schedule: None
  • Marketing Status: Bulk Ingredient For Animal Drug Compounding

Drug Label Information

Updated September 1, 2021

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

View All Sections
  • PRINCIPAL DISPLAY PANEL

    Ponazuril

  • INGREDIENTS AND APPEARANCE
    PONAZURIL 
    ponazuril powder
    Product Information
    Product TypeBULK INGREDIENTItem Code (Source)NDC:10695-093
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    PONAZURIL (UNII: JPW84AS66U) (PONAZURIL - UNII:JPW84AS66U) PONAZURIL1 kg  in 1 kg
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:10695-093-505 kg in 1 CONTAINER09/01/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    BULK INGREDIENT FOR ANIMAL DRUG COMPOUNDING09/01/2021
    Labeler - Willow Birch Pharma, Inc. (617153924)
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!